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Abbott, М.Е. and J. Kaufmann. 1916. Double monster of Janus type: cephalothoracopagus monosymmetros cyclops synotis. Bulletin of the International Association of Medical Museums 6: 95-101
Abramowicz, M.J. et al. 1992. Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goitre. Journal of Clinical Investigation 90: 1200-1204
Abu-Abed, S. et al. 2001. The retinoicacid-metabolising enzyme CYP26A1, is essential for normal hindbrain patterning, vertebral identity and development of posterior structures. Genes and Development 15: 226-240
Addison, J. 1721. The battel [sic] of the pygmies and cranes. London Adelmann, H.B. 1936a. The problem of Cyclopia I. Quarterly Review of Biology II: 161-182
Adelmann, H.B. 1936b. The problem of Cyclopia II. Quarterly Review of Biology II: 284-304
Afzelius, B. 1976. A human syndrome caused by immotile cilia. Science 193: 317-319
Alberch, P. 1986. Possible dogs. Natural History 95: 4-8
Alberts, B. et al. 1994. The molecular biology of the cell. Garland, N.Y.
Albin, R.L. 1988. The pleiotropic gene theory of senescence: supportive evidence from human genetic disease. Ethology and Sociobiology 9: 371-382
Aldrovandi, U. 1642. Monstrorum historia. Bononiae
Ames, B.N. et al. 1993. Oxidants, antioxidants, and the degenerative diseases of ageing. Proceedings of the National Academy of Sciences, USA 90: 7915-7922
Anon. 1829a. Bulletin des sciences médicales 18: 169-172
Anon. 1829b. La Clinique I: 200
Anon. 1829c. La Clinique I: 254-255
Appel, T. 1987. The Cuvier-Geoffroy debate: French biology in the decade before Darwin. Oxford University Press, Oxford, UK
Aristotle. 1984. The complete works of Aristotle: the revised Oxford translation. J. Barnes (ed.) Princeton University Press, Princeton, N.J.
Aterman, K. 1999. From Horus the child to Hephaestus who limps: a romp through history. American Journal of Medical Genetics 83: 53-63
Bachiller, D. et al. 2000. The organiser factors chordin and noggin are required for mouse forebrain development. Nature 403: 658-661
Bacon, F. 1620 (2000). The new organon. L. Jardine and M. Silverthorne (eds) Cambridge Unversity Press, Cambridge, UK
Baker, J.R. 1974. Race. Oxford University Press, N.Y.
Balemans, W. et al. 2001. Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST). Human Molecular Genetics 10: 537-543
Baljet, B. 1990. The cyclopic monsters of the Vrolik collection. Actes du colloque de conservateurs des musées d'histoire des sciences medicales 66-78.
Baljet, B. and M.L. Öjesjö. 1994. Teratology in art or the Dysmorphology Hieronymus Bosch Connection. Actes du 7е colloque des conservateurs des musées d'histore des sciences medicales.
Baljet, B. and R.-J. Oostra. 1998. Historical aspects of the study of malformations in the Netherlands. American Journal of Medical Genetics 77: 91-99
Baljet, B. et al. 1991. Willem Vrolikoncyclopia. Documenta Opthalmologica 77: 355-368
Bamshad, M. et al. 1999. Reconstructing the history of human limb development: lessons from birth defects. Pediatric Research 45: 291-299
Barbin, H. 1980. Herculine Barbin: being the recently discovered memoirs of a nineteenth century French hermaphrodite (intro. M. Foucault, trans. R. McDougall). Pantheon, N.Y.
Barbujani, G. et al. 1997. An apportionment of human DNA diversity. Proceedings of the National Academy of Sciences USA 94: 4516-4519
Barinaga, M. 1993. New protein appears to be long-sought neural inducer. Science 262: 653-254
Barrett, D. and M. McCann. 1980. Two-toed man. Sunday Times Magazine 28-31
Barsh, G. 1999. Of ancient tales and hairless tails. Nature Genetics 22: 315-316
Bartke, A. et al. 2001a. Longevity – extending the lifespan of long-lived mice. Nature 414: 412
Bartke, A. et al. 2001b. Prolonged longevity of hypopituitary dwarf mice. Experimental Gerontology 36: 21-28
Bates, A.W. 2001. The De monstrorum of Fortunio Liceti: a landmark of descriptive teratology. Journal of Medical Biography 9: 49-54
Bateson, W. 1894. Materials for the study of variation. Macmillan, London
Bazopoulou-Kyrkanidou, E. 1997. What makes Hephaestus lame? American Journal of Medical Genetics 72: 144-155
Beckman, K.B. and B.N. Ames. 1998. The free radical theory of ageing matures. Physiological Reviews 78: 547-581
Beddington, R.S.P. 1994. Induction of a second neural axis by the mouse node. Development 120: 613-620
Beddington, R.S.P. and E.J. Robertson. 1999. Axis development and early asymmetry in mammals. Cell 96: 195-209
Bell, A.G. 1918. The duration of life and conditions associated with longevity. Genealogical Record Office, Washington, DC
Bendyshe, T. 1864. On the anthropology of Linnaeus. Memoires of the Anthropological Society of London I: 421-458
Besser, G.M. and M.O. Thorner. 1994. Clinical endocrinology (2nd ed.) Ch. 11. Mosby-Wolfe, London
Betts, D.H. et al. 2001. Reprogramming of telomerase activity and rebuilding of telomere length in cloned cattle. Proceedings of the National Academy of Sciences, USA 98: 1077-1082
Bindman, D. 2002. Ape to Apollo: aesthetics and the idea of race in the eighteenth century. Reaktion, London
Birkett, J. 1858. Congential, supernumerary and imperfectly developed auricles on the sides of the neck. Transactions of the Pathological Society of London 9: 448-449
Bittles, A.H. 2001. Consaguinity and its relevance to clinical genetics Clinical Genetics 60: 89-90
Blair, H.C. 1998. How the osteoclast degrades bone. Bioessays 20: 837-846
Blanchard, R. 1907. Nouvelles observations sur les nègres pies. Geoffroy Satin-Hilaire à Lisbonne. Bulletin de la Société Franсaise d'histoire de la médecine 6: 111-135
Blasco, M.A. et al. 1997. Telomere shortening and tumor formation by mouse cells lacking telomerase RNA. Cell 91: 25-34
Boaistuau, P. 1560 (2000) Histoires prodigieuses, Facsimile of Wellcome MS 136. (S. Bamforth ed.) Franco Maria Ricci, Milan
Boardman, J. 1997a. Pan in text pp. 923-941; plate pp. 612-636 in Lexicon iconographicum mythologiae classicae: VIII: 1 (text); 2 (Plates)
Boardman, J. 1997b. The great god Pan. Thames and Hudson, London
Boas, F. 1912. Changes in bodily form of descendants of immigrants. American Anthropologist 14: 530-562
Bodnar, A.G. et al. 1998. Extension of life-span by introduction of telomerase into normal human cell. Science 279: 349-351
Bogin, B. 1999. Patterns of human growth, 2nd ed. Cambridge University Press, Cambridge. UK
Bonaventure, J. et al. 1996. Common mutations in the Fibroblast Growth Factor Receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia and thanatophoric dwarfism. American journal of Medical Genetics 63: 148-154
Bondeson, J. 1997. A cabinet of medical curiosities. Tauris, London
Bondeson, J. 2000. The two-headed boy and other medical marvels. Cornell University Press, Ithaca. N.Y.
Bondeson, J. and A.E.W. Miles. 1996. The hairy family of Burma: a four generation pedigree of congenital hypertrichosis lanuginosa. Journal of the Royal Society of Medicine 89: 403-408
Bornstein, P.E. and R.R. Peterson. 1966. Numerical variation in the presacral vertebral column in three population groups. American Journal of Physical Anthropology 25: 139-146
Boruwlaski, J. 1792. The Memoirs of the celebrated dwarf Joseph Boruwlaski, A Polish gentleman containing a faithful and curious account of his birth, education, marriage, travels and voyages, (trans. S. Freeman) 2nd ed. J. Thompson. Birmingham
Boulet and Capecchi. 1996. Targeted disruption of Hoxc-4 causes esophageal defects and vertebral transformation. Developmental Biology 177: 232-249
Boyd, W.C. 1955. Genetics and the races of man. Little, Brown and Co., Boston
Brandtt A. 1897. Üeberdiesogenannten Hundemenschen, beziehungsweise über Hypertrichosis universalis. Biologische Zentralblatt 17: 161-179
Broberg, G. 1983. Homo sapiens. Linnaeus' classification of man. in T. Frangsmyr, (ed.) Linnaeus: the man and his work. University of California Press, Berkley
Brockes, J.P. 1998. Regeneration and cancer. Biochimica et biophysica acta. 1377 M1-M11
Brown-Borg, H.M. et al. 1996. Dwarf mice and ageing process. Nature 384: 33
Browne, T. 1904. The works of Thomas Browne. C. Sayle (ed.) Grant Richards, London
Brueckner, M. 2001. Cilia propel the embryo in the right direction. American Journal of Medical Genetics 101: 339-344
Brunet, L.J. et al. 1998. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. Science 280: 1455-1457
Brunkow, M.E. et al. 2001. Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. American Journal of Human Genetics 68: 577-589
Bruyn, G.W. and L.N. Went. 1986. Huntington's Chorea, in Vinken, G. W. et al. (eds.) Extrapyramidal disorders: handbook of clinical neurology 49: 267-273
Buffon, G.L. 1777. Histoire naturelle générale et particulière. Imprimerie Royale, Paris
Burn, J. and T. Strachan. 1995. Human embryo use in developmental research. Nature Genetics 11: 3-6
Callahan, C.A. and A.E. Oro. 2001. Monstrous attempts at adnexogenesis: regulating hair follicle progenitors through sonic hedgehog signalling. Current Opinion in Genetics and Development 11: 541-546
Cargill, M. et al. 1999. Characterisation of single-nucleotidepolymorphisms in coding regions of human genes. Nature Genetics 22: 231-238
Carpenter, E.M. et al. 1993. Loss of Hox-Al (Hox-1.6) function results in the reorganisation of the murine hindbrain. Development 118: 1063-1075
Casey, B. and B.P. Hackett. 2000. Left-right axis malformations in man and mouse. Current Opinon in Genetics and Development 10: 257-261
Cavalli-Sforza, L.L. 1986. The African pygmies. Academic Press, N.Y.
Cavelaars, A.E.J.M. et al. 2000. Persistent variations in average height between countries and between socio-economic groups: an overview of 10 European countries Annals of Human Biology 27: 407-421
Celli, J. et at. 1999. Heterozygous germline mutations in the P53 homolog p63 are the cause of EEC syndrome. Cell 99: 143-151
Chapman, T. and L. Partridge. 1996. Female fitness in Drosophila melanogaster: an interaction between the effect of nutrition and of encounter rates with males. Proceedings of the Royal Society, London Series ВBiological Sciences 263: 755-759
Charlesworth, B. 1996. Evolution of senescence: Alzheimer's disease and evolution. Current Biology 6: 20-22
Chen, L. et al. 2001. A Ser{j65)->Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates ihh / PTHrP signals and causes severe achondroplasia. Human Molecular Genetics 10: 457-465.
Chen, Y. et al. 2000. Conservation of early odontogenetic signaling pathways in Aves. Proceedings of the National Academy, USA 97: 10044-10049
Chiang, C. et at. 1996. Cyclopia and defective axial patterning in mice lacking sonic hedgehog gene function. Nature 383: 407-412
Chiang, C. et al. 2001. Manifestation of the limb prepattern: limb development in the absence of sonic hedgehog function. Developmental Biology 236: 421-435
Chisaka, O. and M.R. Capecchi. 1991. Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5 (HoxA3). Nature 350: 473-479
Cibelli, J.B. et at. 2002. The health profile of cloned animals. Nature Biotechnology 20: 13-14
Clark, R.M. et al. 2001. Reciprocal mouse and human limb phenotypes caused by gain and loss-of-function mutations affecting Lmbn. Genetics 159: 715-726
Coates, M.I. and J.A. Clack. 1990. Polydactyly in the earliest tetrapod limbs. Nature 347: 66-69.
Cockayne, E.A. 1933. Inherited abnormalities of the skin and its appendages. Oxford University Press, London
Cohen, M.M. 2002. Bone morphogenetic proteins with some comments on fibrodysplasia ossificans progressiva. American Journal of Medical Genetics 109: 87-92
Cohen, M.M. 1988. Further diagnostic thoughts about the Elephant Man. American Journal of Medical Genetics 29: 777-782
Cohen, M.M. 1989. A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Advances in Human Genetics 18: 181-303
Cohen, M.M. 1993. Proteus syndrome: clinical evidence for somatic mosaicism and selective review. American Journal of Medical Genetics 47: 645-652
Cohen, M.M. 2001. Problems in the definition of holoprosencephaly. American Journal of Medical Genetics 103: 183-187
Cohen, M.M. and K. Shiota. 2002. Teratogenesis of holoprosencephaly. American Journal of Medical Genetics 109: 1-15
Cohn, M.J. and C. Tickle. 1999. Developmental basis for limblessness and axial patterning in snakes. Nature 399: 474-479
Cohn, M.J. and P.E. Bright. 2000. Development of vertebrate limbs: insight into pattern, evolution and dysmorphogenesis. in O'Higgins, P. and M.J. Cohn (eds) Development, growth and evolution: implications for the hominidskeleton. Academic Press, N.Y.
Collins-Schramm, H.E. 2002. Ethnic-difference markers for use in mapping by admixture linkage disequilibrium. American Journal of Human Genetics 70: 737-750
Colvin, J.S. et al. 1996. Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3. Nature Genetics 12: 391-397
Comfort, A. 1964. Ageing: the biology of senesence. Holt, Rinehart and Winston. N.Y.
Conner, M. and M. Ferguson-Smith. 1993. Essentials of medical genetics. (5th ed.) Blackwell Science, Oxford
Conte, E A. et a I. 1994. A syndrome of female pseudohermaphroditism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450 arom). Journal of Clinical Endocrinology and Metabolism 78: 1287-1292
Corcoran, J. 1998. What are the molecular mechanisms of neural tube defects? Bioessays 20: 6-8
Corder, E.H. et al. 1993. Gene dose ofapololipoprotein E Type 4 allele and the risk of Alzheimer's disease in late onset families. Science 261: 921-923
Cornaro, L. 1550 (1903). The art of living long: a new and improved English version of the treatise by the celebrated Venetian centenarian, Louis Cornaro with Essays by Joseph Addison, Lord Bacon and Sir William Temple. W.E Butler, Milwaukee
Cotsarelis, G. and S.E. Millar. 2001. Towards a molecular understanding of hair loss and its treatment. Trends in Molecular Medicine 7: 293-301
Crackower, M.A. et al. 1998. Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse. Developmental Biology 201: 78-89
Crawfurd, J. 1827. Journal of an embassy from the Governor-General of india to the court of Ava in the year 1827. V.1. H. Colburn. London
Crosby, J.L. et al. 1992. Disorganisation is a completely dominant gainoffunction mouse mutation causing sporadic developmental defects. Mechanisms of Development 37: 121-126
Crow, J.E. 2000. The origins, patterns and implications of human spontaneous mutation. Nature Reviews Genetics I: 40-47
Danerow, H. 1830. Ueber Ritta-Christina und die Siamesen. Litterarishcen Annaleen dergesammten Heilkunde 16: 454-482
Darwin, C. 1859 (1968). The origin of species by means of natural selection. Penguin, Harmondsworth, UK
Darwin, C. 1871 (1981). The descent of man, and selection in relation to sex. Princeton University Press, Princeton, N.J.
Darwin, C. 1882. The variation of animals and plants under domestication, 2nd ed. John Murray, London
Dasen, V. 1993. Dwarfs in ancient Egypt and Greece. Clarendon Press, London
Dasen, V. 1994. Pygmaioi. text p.594-601; plates p.466-486. Lexicon Iconographicum Mythologiae Classicae VIII: 1 (text); 2 (plates)
Dasen, V. 1997. Multiple births in Graeco-Roman antiquity. Oxford Journal of Archaeology 16: 49-61
Dasen, V. 2002. Les jumeaux siamois dans l'Antiquite classique: du my the au phenomene de foire. La Revue du Practicien 52: 9-12
Daston, L. and K. Park. 1998. Wonders and the order of nature 1150-1750. Zone, N.Y.
De Luca, F. and J. Baron. 1999. Control of bone growth by fibroblast growth factors. Trends in Endocrinology and Metabolism 10: 61-65
De Quatrefages, A. 1895. The pygmies (trans. F. Starr). Macmillan, London
De Vijlder, J. et al. 1999. Defects in thyroid hormone supply. Ch. 16b. The Thyroid and its Diseases:
Del Campo, M. et al. 1999. Mondactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster. American Journal of Human Genetics 65: 104-110
Delange, F. and B. Hetzel. 2000. The iodine Deficiency Disorders. Ch. 20. The Thyroid and Its Diseases:
DeRobertis, E. and Y. Sasai. 1996. A common plan for dorsoventral patterning in Bilateria. Nature 380: 37-40
Diamond, J.M. 1982. Big-bang reproduction and ageing in male marsupial mice. Nature 298: 115-116
Diamond, J.M. 1991. Why are pygmies so small? Nature 354: 111-112
Didde, R. 2002. Wetenschap. Volkskrant 25 May 2002
Dikötter, F. 1992. The discourse of race in modern China. Hurst, London
Dikötter, F. 1997. Hairy barbarians, furry primates, and wild men: medical science and cultural representations of hair in China, in Hiltebeitel, A. and B. D. Miller (eds) Hair: its power and meaning in Asian cultures. SUNY Press, Albany, N.Y.
Dikötter, F. 1998. Imperfect conceptions: medical knowledge, birth defects, and eugenics in China. Hurst, London
Dobson, J. 1958. Marie Sabina, the variegated damsel. Annals of the Royal College of Surgeons 22: 273-278
Dolle, P. et al. 1993. Disruption of the Hoxd-13 gene induces localised heterochrony leading to mice with neotenic limbs. Cell 75: 431-441
Donnai D. and R.M. Winter. 1989. Disorganisation: a model for 'early amnion rupture'? Journal of Medical Genetics 26: 421-425.
Dreger, A.D. 1998. Hermaphrodites and the medical invention of sex. Harvard University Press. Cambridge, Mass.
Dudley, A.T. et al. 2002. A re-examination of proximodistal patterning during vertebrate development. Nature 418: 539-544
Durham-Pierre, D. et al. 1994. African origin of an intragenic deletion of the human P gene in tyrosine positive oculocutaneous albinism. Nature Genetics 7: 176-179
Egenvall, A. et al. 2000. Age pattern of mortality in eight breeds of insured dogs in Sweden. Preventative Veterinary Medicine 46: 1-14
Eigenmann, J.E. 1987. Insulin-like growth factor 1 in dogs. Frontiers of Hormone Research 1 7: 161-172
Eigenmann, J.E. et al. 1988. Insulin-like growth factor 1 levels in proportionate dogs, chondrodystrophic dogs and in giant dogs. Acta Endocrinologica (Copenhagen) 118: 105-108
Eigenmann J.E. et al. 1984. Body size parallels insulin-like growth factor 1 levels but not growth hormone secretory capacity. Acta Endocrinologica (Copenhagen) 106: 448-453
Emery, A.E.H. 1996. Genetic disorders in portraits. American Journal of Medical Genetics 66: 334-339
Epstein, C.J. et al. 1987. Transgenic mice with increased Cu7/jZn-superoxide dismutase activity: animal model of dosage effects in Down syndrome. Proceedings of the National Academy of Sciences USA 84: 8044-6048
Eyre-Walker, A. and P.D. Keightley. 1999. High genomic deleterious mutation rates in hominids. Nature 397: 334-347
Farrell, H.B. 1984. The two-toed Wadoma – familial ectrodactyly in Zimbabwe. South African journal of Medicine 65: 531-533
Fasseler, P.E. and K. Sander. 1996. Hilde Mangold (1898-1924) and Spemann's organiser: Achievement and Tragedy. Wilhelm Roux Archives of Developmental Biology 205: 323-332
Felgenhauer, W.-R. 1969. Hypertrichosis lagnuinosa universalis. Journal de Genetique humaine 17: 1-44
Ferretti, P. and C. Tickle. 1997. The limbs, in P. Thorogood (ed.) Embryos, genes and birth defects. John Wiley and Sons, N.Y.
Figuera, L.E. 1995. Mapping of the congenital generalised hypertrichosis locus to chromosome Xq24-q27.1. Nature Genetics 10: 202-206
Finch, C.E. 1990. Longevity; senescence and the genome. Chicago University Press
Finch, C.E. and G. Ruvkun. 2001. The genetics of ageing. Annual Reviews of Genomics and Human Genetics 2: 435-462
Fischer; J.L. 1972. Le concept expérimental dans I'oeuvre tératologique d'Etienne Geoffroy Saint-Hilaire. Revue d'histoire des sciences 25: 347-362
Fischer, J.L. 1991. Monstres: histoire du corps etde ses défauts. Syros, Paris
Flanagan, N. et al. 2000. Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation. Human Molecular Genetics. 9: 2531-2537
Flatt, A.E. 1994. The care of congenital hand anomalies. Quality Medical Publishing. St Louis. Mo.
Fleischer, R. 1984. Artemis Ephesia. text PP 755-63; plates PP.564-73 in Lexicon iconographicum mythologiae classicae II: I (text); 2 (plates)
Flurkey, K. et al. 2001. Lifespan extension and delayed immune and collagen aging in mutant mice with defects in growth hormone production. Proceedings of the National Academy of Sciences USA 98: 6736-6741
Forbes, L.S. 1997. The evolutionary biology of spontaneous abortion in humans. Trends in Ecology and Evolutionary Biology 12: 446-450
Frank, L.G. 1997. Evolution of genital masculinisation: why do female hyenas have such a large 'penis'? Trends in Ecology and Evolution 12: 58-62
Frankcom, G. and J.H. Musgrave. 1976. The Irish giant. Duckworth, UK
Fraser, G. 1877. Wigtown and Whithorn: historical and descriptive sketches, stories and anecdotes, illustrative of the racy wit and pawky humour of the district. Gordon Fraser, Wigtown
Fraumeni, J.F. 1967. Stature and malignant tumors of bones in childhood and adolescence. Cancer 20: 967-973
Freire-Maia, A. 1975. Genetics of acheiropodia (the handless and footless families of Brazil). VI. Formal genetic analysis. American Journal of Human Genetics 27: 521-527
Freire-Maia, A. 1981. Historical note: The extraordinary handless and footless families of Brazil – 50 years of acheiropodia. American Journal of Human Genetics 9: 31-41
Frey, J. 1994. Toulouse-Lautrec: a lift. Weidenfeld and Nicolson, London
Frey, J. 1995a. What dwarfed Toulouse-Lautrec? Nature Genetics 10: 128-130
Frey, J. 1995b. Toulouse-Lautrec's diagnosis – reply. Nature Genetics 11: 363
Friedman, J.B. 1981. The monstrous races in medieval thought and art. Harvard, Cambridge, Mass.
Fromental-Ramain, C. et al. 1996. Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the autopod. Development 122: 2997-3011
Fullerton, S.M. et al. 2000. Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism. American Journal of Human Genetics 67: 881-900
Galis, F. 1999. Why do almost all mammals have seven cervical vertebrae? Developmental constraints, Hox genes, and Cancer. Journal of Experimental Zoology 285: 19-26
Galis, F. 2001. Why five fingers? Evolutionary constraints on digit number. Trends in Ecology and Evolution. 16: 637-646
Garcia-Cruz D. et al. 2002. Inherited hypertrichoses. Clinical Genetics 61: 321-329
Gat, U. et al. 1998. De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated Beta-catenin in skin. Cell 95: 605-614
Gates, R.R. 1961. The Melanesian dwarf tribe of Aiome, New Guinea. Acta Geneticae Medicae et Gemellogiae. 10: 277-311
Geffner, M.E. et al. 1995. Insulin-like growth factor I resistance in immortalised T cell lines from African Efe pygmies. Journal of Clinical Endocrinology and Metabolism. 80: 3732-3738
Geffner, M.E. et al. 1996. IGF-ldoes not mediate T lymphoblast colony formation in response to estradiol, testosterone, 1,25(OH)2, Vitamin D3 and triiodothyronine; studies in control and pygmy lines Biochemical and Molecular Medicine 59: 72-79
Gegenbauer, C. 1880. Critical remarks on polydactlyly as atavism. Morphologisches Jahrbuch 6: 584-596
Gehring, W. and K. Ikeo. 1999. Pax 6: mastering eye morphogenesis and eye evolution. Trends in Genetics 15: 371-377 
Geissler, W. et a I. 1994. Male pseudohermaphroditism caused by mutations of testicular 17-beta-hydroxysteroid dehydrogenase 3. Nature Genetics 7: 35-39
Gelb, D. et al.1996. Pycnodysostosis, a lysosomal disease caused by Cathepsin K deficiency. Science 273: 1236-1239
Gelfland, M., C.J. Roberts, and R.S. Roberts. 1974. A two-toed man from the Doma people of the Zambezi Valley. Rhodesian History 5: 92-95
Geoffroy Saint-Hilaire, E. 1822. Philosophie anatomique des monstruosités humaines. Deville-Cavellin, Paris
Geoffroy Saint-Hilaire, E. 1829. Rapport sur le monstre bicéphale Ritta-Christina. Gazette de Sante (No. 270)
Geoffroy Saint-Hilaire, E. 1838. Notions synthétiques, historiques et physiologiques de Philosophie Naturelle. Denain, Paris
Geoffroy Saint-Hilaire, I. 1832-37. Histoire générale et particulière des anomalies de l'organisation chez l'homme et les animaux. J.B. Balliere, Paris
Geoffroy Saint-Hilaire, I. 1847. Vie, travaux et doctrine scientifique d'Étienne Geoffroy Saint-Hilaire. La Societe Geologique de France, Paris
Gerhart, J. 2000. Inversion of the chordate body axis: Are their alternatives? Proceedings of the National Academy of Sciences, USA 97: 4445-4448
Gertz, O. 1948. Artemis och hinden frontispisplanschen Linnes Fauna Svecica. Svenska Linne-Sallskapets Arsskrift 31: 13-37
Gilbert, S.F. 2000. Developmental biology (6th edition). Sinauer Associates, Sunderland, Mass.
Glass, B. 1947. Maupertuis and the beginning of genetics. Quarterly Review of Biology 22: 196-210
Glickman, S.E. et al. 1992. Hormonal correlates of 'masculinisation' in female spotted hyenas (Crocuta crocuta). 1. Infancy to sexual maturity. Journal of Reproduction and Fertility 95: 451-462
Goding, C.R. 2000. Mitf from neural crest to melanoma: signal transduction and transcription in the melanocyte lineage. Genes and Development 14: 1712-1728
Gong, Y. et al. 1999. Heterozygous mutations in the gene encoding noggin affect human morphogenesis. Nature Genetics 21: 302-304
Goto, N. et al. 1987. The mexican hairless dog, its morphology and inheritance. Experimental Animals (Tokyo) 36: 87-90
Goujon, E. 1869. Étude d'un cas d'hermaphrodisme bisexuel imparfait chez l'homme. Journal de Tanatomie et de la physiologie normales et pathologiques de Thomme et des animaux 6: 599-616
Gould, G.M. and W. L. Pyle. 1897. Anomalies and curiosities of medicine. W.B. Saunders, Philadelphia
Gould, S.J. 1981. The mismeasure of man. W.W. Norton, N.Y.
Gould, S.J. 1983. Hen's teeth and horse's toes. W.W. Norton, N.Y.
Graves, J.A. 1998. Interactions between SRY and SOX genes in mammalian sex determination. Bioessays 20: 264-269
Gravlee, C.G. et al. 2003. Heredity, environment and cranial form: a reanalysis of Boas's Immigrant data. American Anthropologist 105: 125-138
Gruber, G.B. 1955. Historisches und aktuelles iiberdas Sirenen-problem in der medizin. Nova Acta Leopoldina 17: 89-122
Gruman, G.J. 1966. A history of ideas about the prolongation of life. Transactions of the American Philosophical Society 56: 1-102
Gubbay, J. et al. 1990. A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes. Nature 346: 245-250
Guichard, C. et al. 2001. Axonemal dyneinintermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskenesia (Kartagener syndrome). American Journal of Human Genetics 68: 1030-1035
Gunther, T. and T. Schinke. 2000. Mouse genetics have uncovered new paradigms in bone biology. Trends in Metabolism. II: 189-193
Guyda, H.J. 1998. Growth hormone therapy for non-growth hormone-deficient children with short stature. Current Opinion in Pediatrics 10: 416-421
Haldane, J.B.S. 1941. New paths in genetics. George Allen & Unwin, London
Hale, F. 1933. Pigs born without eyeballs. Journal of Heredity 24: 105-106
Haliburton, R.G. 1891. The dwarfs of Mount Atlas. David Nutt, London
Haliburton, R.G. 1894. Survivals of dwarf races in the new world. Proceedings of the American Association for the Advancement of Science 14: 1-14
Hall, B.K. 1995. Atavisms and atavistic mutations. Nature Genetics 10: 126-127
Hamburger, V. 1947. Monsters in nature. Ciba Symposia 9: 666-683
Hamburger, V. 1988. The heritage of experimental embryology: Hans Spemann and the organiser. Oxford University Press
Hamilton, J.В. 1942. Male hormone stimulation is a prerequisite and an incitant in common baldness. American Journal of Anatomy 71: 451-480
Hanihara, T. 2000. Frontal and facial flatness of major human populations. American Journal of Physical Anthropology 111: 105-134
Haraguchi, R. et al. 2000. Molecular analysis of external genitalia formation: the role of fibroblast growth factor (FGF) genes during genital tubercle formation. Development 127: 2471-2479
Harding, R.M. et al. 2000. Evidence for variable selective pressure at MC1R American Journal of Human Genetics 66: 1351-1361
Hardy, M.H. 1992. The secret life of the hair follicle. Trends in Genetics 8: 55-61
Harrison, R.G. 1924. Some unexpected results of the heteroplastic transplantation of limbs. Proceedings of the National Academy of Sciences, USA 10: 69-74
Harvey, R.G. and D.R Brothwell. 1969. Biosocial aspects of Ainu hirsuteness. Journal of Biological Sciences 1: 109-124
Harvey, W. 1965. The works of William Hartley. Willis, R (ed., trans.) Sydenham Society, London
Haupt, H. et al. 1990. Le bestiaire de Rodolphe II. (trans. L. Marcou) Citadelles, Paris
Hayashizaki, Y. et al. 1989. Thyroid-stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the β-subunit. EMBO Journal 8: 2291-2296 
Headon, D.J. and P.A. Overbeek. 1999. Involvement of a novel Tnf receptor homologue in hair follicle induction. Nature Genetics 22: 370-374
Healy, E. et al. 2001. Functional variation of MC1R alleles from red-haired individuals. Human Molecular Genetics. 10: 2397-2402
Heijmans, B.T. et al. 2000. Common gene variants, mortality and extreme longevity in humans. Experimental Gerontology 35: 865-877
Hennessy, R.J. and C.B. Stringer. 2002. Geometric morphometric study of the regional variation of modern human craniofacial form. American Journal of Physical Anthropology 117: 37-48
Herdt, G. 1994. Mistaken sex: culture, biology and the third sex in New Guinea, in G. Herdt (ed.) Third sex, third gender. Zone Books. Cambridge, Mass.
Heron, T.M. 1986. Boruwlaski, the little count. Durham, UK
Hertel, C. 2001. Hairy issues: Portraits of Petrus Gonsalus and his family in Archduke Ferdinand II's Kunstkammer and their contexts. Journal of the History of Collections 13: 1-22
Hinchliffe, J.R. and D.R.Johnson. 1980. The development of the vertebrate limb. Claredon Press, Oxford
Holekamp, K.E. et al. 1996. Rank and reproduction in female spotted hyenas. Journal of Reproduction and Fertility 108: 229-237
Holliday, R. 1989. Food, reproduction and longevity: is the extended lifespan of calorie-restricted animals an evolutionary adaptation? Bioessays 10: 125-127
Holly, J.M.P. et al. 1999. Growth hormone, IGF-1 and cancer. Less intervention to avoid cancer? More intervention to prevent cancer? Journal of Endocrinology 162: 321-330
Horan,. G.S. et al. 1994. Homeotic transformation of cervical vertebrae in Hoxa-4 mutant mice. Proceedings of the National Academy of Sciences, USA. 91: 12644-12648
Horan, G.S. et al. 1995a. Compound mutants for the paralogous Hoxa-4, Hoxb-4, and Hoxc-4 genes show more complete homeotic transformations and a dose dependent increase in the number of vertebrae transformed. Genes and Development 9: 1667-1677
Horan, G.S. et al. 1995b. Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton-evidence for unique and redundant function. Developmental Biology 169: 359-372
Houssay, E. 1937. De la nature, des causes, des différences des monstres. Editions Hippocrates, Paris
Hu, D. and J.A. Helms. 1999. The role of sonic hedgehog in normal and abnormal craniofacial morphogenesis. Development 126: 4873-4884
Huelsken J. et al. 2001. Beta-catenin controls hair follicle morphogenesis and stem cell differentiation in the skin. Cell 105: 533-545
Hummel, K.P. 1958. The inheritance and expression of Disorganization, an unusual mutation in the mouse. Journal of Experimental Zoology 137: 389-423
Hummel, K.P. 1959. Developmental anomalies in mice resulting from action of the gene Disorganization, a semi-dominant lethal. Pediatrics 23: 212-221
Ianakiev, P. et al. 2000. Acheiropodia is caused by a g~nomic deletion in C70rf2 the human orthologue of the Lmbr1 gene. American Journal of Human Genetics 68: 38-45
Imperato-McGinley, J. et al. 1974. Steroid 5-alpha-reductase deficiency in man: an inherited form of male pseudohermaphroditism. Science 186: 1213-1215
Imperato-McGinley, J. et al. 1991. A cluster ofmale pseudohermaphrodites with 5-alpha-reductase deficiency in Papua New Guinea. Clinical Endocrinology 34: 293-298
Incardona, J.P. 1998. The teratogenic Veratrum alkaloid cyclopamine inhibits sonic hedgehog signal transduction. Development 125: 3553-3562
International Sequencing Consortium. 2001. Initial sequencing and analysis of the human genome. Nature 409: 860-921
Irving, J. 1862. The drowned women of Wigton, a romance of the Covenant. Porteous and Hislop, Glasgow
Isaac, A. et al. 2000. FGF and genes encoding transcription factors in early limb specification. Mechanisms of Development 93: 41-48
Iwai, T. 1907. A statistical study on the polymastia of the Japanese. Lancet 2: 753-4
Jackson, I.J. 1997. Homologous pigmentation mutations in human, mouse and other model organisms. Human Molecular Genetics 6: 1613-1624
Jackson, W.P.U. 1951. Osteo-dental dysplasia (Cleidocranial dysostosis) 'The Arnold Head'. Acta Medica Scandinavica 139: 293-295
Janin, J. 1829. (1998) Une femme à deux têtes. S. Pestel (ed.) La collection electronique de la Biblioteque Municipale de Lisieux:
Jarvik, G.P. et al. 1994. Non-mendelian transmission in a human developmental disorder: Split Hand / Split Foot. American Journal of Human Genetics 55: 710-713
Jeannotte, L. et al. (1993) Specification of axial identity in the mouse: role of the Hoxa5 (Hox1.3) gene. Genes and Development 7: 2085-2096
Jenkins, P. 1998. Cancer in acromegaly. Trends in Endocrinology and Metabolism 9: 360-366
Johanson, D. and B. Edgar. 1996. From Lucy to language. Orion, London
Joseph, R. and P. Godson. 1988. Peace at last for tragic Rita: white outcase in black skin. Sunday Times Johannesburg). 28 August, p. 12
Jost, A. 1946-47. Recherches sur la différenciation sexuellede l'етbryоп de lapin (Troisieme Partie). Archives d'anatomie microscopique et de morphologie expérimental 36: 271-315
Jung, H.-S. et al. 1998. Local inhibitory action of BMPs and their relationships with activators in feather formation: implications for periodic patterning. Developmental Biology 196: 11-23
Kappler, С. 1980. Monstres, demons et merveilles a la fin du Moyen age. Payot, Paris
Kaufman, M.H. and K.S. O'Shea. 1978. induction of monozygotic twinning in the mouse. Nature 276: 707-708
Keith, A. 1911. An inquiry into the nature of the skeletal changes in acromegaly Lancet 1: 993-1002
Kenyon, C. et al. 1993. АС. elegans mutant that lives twice as long as wild type. Nature 366: 461-464
Kere, J. et al. 1996. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by a mutation in a novel transmembrane protein. Nature Genetics 13: 409-416
Kingdon-Ward, F. 1924. From China to Hkamti Long. Edward Arnold, London
Kingdon-Ward, F. 1937. Plant hunter's paradise. Jonathan Cape, London
Kirk, G.S. 1974. The nature of the Greek myths. Penguin, Harmondsworth, UK
Knussmann, R. et al. 1992. Relations between sex hormone level and characteristics of hair and skin in healthy young men. American Journal of Physical Anthropology 88: 59-67
Kobelt, G.L. 1844. The female sex organs in humans and some mammals (trans. H.E Bernays) in Lowry, T.P. (1978) The classic clitoris, historical contributions to scientific sexuality. Nelson-Hall, Chicago
Kohn, M. 1995. The race gallery: the return of racial science. Jonathan Cape, London
Kollar, E.J. and C. Fisher. 1980. Tooth induction in chick epithelium: expression of quiescent genes for enamel synthesis. Science 207: 993-995
Komori et al. 1997. Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts. Cell 89: 755-764
Kondo, S. et al. 2001. The medaka rS-3 locus required for scale development encodes ectodysplasin-A receptor. Current Biology 7: 1201-1206
Kondo, T. et al. 1997. Of fingers, toes, and penises. Nature 390: 29
Koren, Y. and E. Negev. 2003. im Herzen waren wir Riesen. Econ, Munich
Kornak, U. et al. 2000. Mutations in the а3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis. Human Molecular Genetics 9: 2059-2063
Kostic, D. and M.R. Capecchi. 1994. Targeted disruptions of the murine HoxA-4 and HoxA-6 genes result in homeotic transformations of components of the vertebral column. Mechanisms of Development 46: 231-247
Kremer, H. et al. 1995. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinising hormone receptor gene. Nature Genetics 9: 160-164
Krude, H. et al. 1998. Severe early onset obesity, adrenal insufficiency and red hair pigmentation caused by РОМС mutations in humans. Nature Genetics 19: 155-157
Kruglyak, L. and D.A. Nickerson. 2001. Variation is the spice of life. Nature Genetics 27: 234-236
Krzisnik, C. et al. 1999. The 'Little People' of the Island of Krk – Revisited. Etiology of hypopituitarism revealed. Journal of Endocrine Genetics 1: 9-19
Kuester and Happle. 1984. The inheritance of common baldness. Two В or not two B? Journal of the American Academy of Dermatology 11: 921-926
Laara, E. and P. Rantakallio. 1996. Body size and mortality in women: a 29-year follow up of 12,000 pregnant women in northern Finland. Journal of Epidemiology and Community Health 50: 408-414
Lahr, M.M. 1996. The evolution of modern human diversity: a study in cranial variation. Cambridge University Press
Lamb, T.M. et al. 1993. Neural induction by the secreted polypeptide noggin. Science 262: 713-718
Lammer, E.J. et al. 1985. Retinoicacid embryopathy. New England Journal of Medicine 313: 837-841
Landucci, L. 1542, 1927. A Florentine diary from 1450 to 1516 by Luca Landucci, continued by an anonymous writer till 1542 with notes by lodoco del Badia (trans. A. de Rosen Jervis). J.M. Dent & Sons, London
Lanza, R.P. et al. 2000. Extension of cell life-span and telomere length in animals cloned from senescent somatic cells. Science 288: 665-668
Laqueur, T.W. 1989. 'Amor Veneris, vel Dulcedo Appeleteur' pp.90-131 in M. Feher (ed.) Zone 5. Fragments for a history of the human body, part 3. Zone, N.Y.
Laqueur, T.W. 1990. Making sex, body and gender from the Greeks to Freud. Harvard University Press, Cambridge. Mass.
Laue, L.L. et al. 1996. Compound heterozygous mutations of the luteinising hormone receptor gene in Leydig cell hypoplasia. Molecular Endocrinology 10: 987-997
Lawrence, P. 1992. The making of a fly. Blackwell. London
Laycock, J. and P. Wise. 1996. Essential Endocrinology. (3rd ed.) Oxford University Press
Lazner, E. et al. 1999. Osteopetrosis and osteoporosis: two sides of the same coin. Human Molecular Genetics 8: 1839-1846
Le Guyader, H. 1998. Etienne Geoffroy Saint-Hilaire (1772-1844): un naturalist visionnaire. Belin, Paris
Le Mouellic, H. et al. 1992. Homeosis in the mouse induced by a null mutation in the HOX-3.1 gene. Cell 69: 251-264
Le Roith, D. et al. 2001. What is the role of circulating IGF? Trends in Endocrinology and Metabolism 12: 48-52
Lee, C.-K. et al. 1999. Gene expression profile of aging and its retardation by caloric restriction. Science 285: 1390-1393
Lee, H.W. et al. 1998. Essential role of mouse telomerase in highly proliferative organs. Nature 392: 569-574
Lee, P.A. and S.R Witchel. 1997. The influence of estrogen on growth. Current opinion in pediatrics 9: 431-436
Lenz, W. 1962. Thalidomide and congenital abnormalities. Lancet 1: 45
Leroi, A.M. 2001. Molecular signals versus the loi de balancement. Trends in Ecology and Evolution. 16: 24-29
Leroi, A.M. et al. 2003. Cancer selection. Nature Cancer Reviews 3: 226-231
Lettice, L.A. et al. 2002. Disruption of a long-range cis-acting regulator for Shh causes preaxial Polydactyly. Proceedings of the National Academy of Sciences; USA 99: 7548-7553
Levin, M. et al. 1995. A molecular pathway determining left-right asymmetry in chick embryogenesis. Cell 82: 803-814
Levin, M. et al. 1996. Laterality defects in conjoined twins. Nature 384: 321
Lewandoski, M. et al. 2000. Fgf8 signalling from the AER is essential for normal limb development. Nature Genetics 26: 460-463
Lewis, E. 1978. A gene complex controlling segmentation in Drosophila. Nature 27: 565-570
Lewis, T. and D. Embleton. 1908. Split-hand and split-foot deformities, their types, origin, and transmission. Biometrika 6: 26-58
Li, J. et al. 1997. Dinucleotide repeat in the 3' flanking region provides a clue to the molecular evolution of the Duffy gene. Human Genetics 99: 573-577
Liceti, F. 1634. De monstrorum natura caussis et differentiis. Padua
Licht, P. et al. 1992. Hormonal correlates of 'masculinisation' in female spotted hyenas (Crocuta crocuta). 2. Maternal and fetal steroids. Journal of reproduction and fertility 95: 463-474
Lickert, H. et al. 2002. Formation of multiple hearts in mice following deletion of beta-catenin in the embryonic endoderm. Developmental Cell 3: 171-181
Lifton, R.J. 1986. The Nazi doctors: medical killing and the psychology of genocide. Macmillan, London
Lindroth, S. 1983. The two faces of Linnaeus. in T. Fdingsmyr (ed.) Linnaeus: the man and his work. University of California Press, Berkeley
Linnaeus, C. 1758, 1939. Systema naturae. 10th edition. British Museum, London
Linnaeus, C. 1761. Fauna svecica. Stockholm
Lloyd, A.T. 1986. Pussy Cat, Pussy Cat, where have you been? Natural History 95(7): 46-52
Logrofio, R. et al. 1997. Heteropagus conjoined twins due to fusion of two embryos: report and review. American Journal of Medical Genetics 73: 239-243
Lopez-Bermejo, A. et al. (2000). Genetic defects of the growth hormone-insulin-like growth factor axis. Trends in Endocrinology and Metabolism 11: 39-49
Lufkin, T. et al. 1991. Disruption of the Hox-1.6 (Hoxal) homeobox gene results in defects in a region corresponding to its rostral domain of expression. Cell 66: 1105-1119
Lupu, F. et al. 2001. Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. Developmental Biology 229: 141-162
McBride,W.B. 1961. Thalidomide and congenital abnormalities. Lancet 11: 1358
McEwan, C. et al. 1997. (eds) Patagonia: natural history, prehistory and ethnography at the uttermost ends of the earth. British Museum, London
Mackenbach, J.P. 1991. Narrowing inequalities in children's height. Lancet 338: 764
McLachlan, J. 1994. Medical embryology: Addison-Wesley, Wokingham
McLaren, A. 1990. What makes a man a man? Nature 346: 216-217
McMahon J.A. et al. 1998. Noggin-mediated antatonism of BMP signalling is required for growth and patterning of the neural tube and somite. Genes and Development 12: 1438-1452
McMullen, G. and K. Pearson. 1913. On the inheritance of the deformity known as split-foot or lobster-claw. Biometrika 9: 381-390
McPherron, A.C. and S.J. Lee. 1997. Doubling muscle in cattle due to mutations in the myostatin gene. Proceedings of the National Academy of Sciences, USA 94: 12457-12461
McPherron, A.C. et a 1.1997. Regulation of skeletal muscle mass in mice by a new TGF-Beta superfamily member. Nature 387: 83-90
Maden, M. 1999. Heads or tails? Retinoic acid will decide. Bioessays 21: 809-812
Maeder, T. 1998. A few hundred people turned to bone. The Atlantic, February, (two parts)
Manoiloff, E.O. 1931. A rare case of hereditary hexadactylism. American Journal of Physical Anthropology 15: 503-508
Manouvrier-Hanu S. et al. 1999. Genetics of limb anomalies in humans. Trends in Genetics 15: 409-417
Mansholt, U.J. 1987. The increase in the height of Dutchmen and the attraction of tennis. Nederlands Tijdschrift voor Geneeskunde 131: 376
Mark, M. et al. 1993. Two rhombomeres are altered in Hoxa-I mutant mice. Development 119: 319-338
Maroteaux,P. 1995. Toulouse-Lautrec's diagnosis. Nature Genetics II: 362
Maroteaux, P. and M. Lamy. 1965. The malady of Toulouse-Lautrec. JAMA, Journal of the American Medical Association 191: 111-113
Marshall, H.K. and H.I. Harder. 1958. Testicular feminising syndrome in male pseudohermaphrodite: report of two cases in identical twins. Obstetrics and Gynecology 12: 284-293
Martin, E. 1880. Histoire des monstres. C. Reinwald, Paris
Martin, G. and J. Oshima. 2000. Lessons from human progeroid syndromes. Nature 408: 263-266
Martinez-Frias, M.-L. 1993. Another way to interpret the description of the Monster of Ravenna of the sixteenth century. American Journal of Medical Genetics 49: 362
Mascie-Taylor, C.G.N. and J.L. Boldsen. 1985. Regional and social analysis of height variation in a contemporary British sample. Annals of Human Biology 12: 315-324
Mathon, N.F. et al. 2001. Lack of replicative sensecence in normal rodent glia. Science 291: 872-875
Mayor, A. 2000. The first fossil hunters. Princeton University Press, Princeton, N.J.
Medawar, P.B. 1952. An unsolved problem in biology. H. K. Lewis. London
Melanchthon, P. and M. Luther. 1523 (1823). Interpretation of two horrible monsters [Deuttung tier czwo grewlichï Figuren, etc.]
Merimee, T.J. et al. 1981. Dwarfism in the pygmy. New England Journal of Medicine 305: 965-968
Merimee, T.J. et al. 1987. Insulin-like growth factors in pygmies: the role of puberty in determining final stature. New England Journal of Medicine 316: 906-911
Merke, F. 1993. History and iconography of endemic goitre and cretinism. MTP Press, Lancaster
Merlo, G.R. et al. 2002. Mouse model of split hand / foot malformation type 1. Genesis 33: 97-101
Meyers, E.N. and G.R. Martin. 1999. Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH. Science 285: 403-406
Miller, R. and S. Austad. 1999. Large animals in the fast lane. Science 285: 199
Mills, A.A. et al. 1999. p63 is a P53 homologue required for limb and epidermal morphogenesis. Nature 398: 708-713
Mittwoch, U. 1973. Genetics of sex differentiation. Academic Press, N.Y.
Monreal, A.W. 1999. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genetics 22: 366-369
Montaigne, M. de. 1580 (1958). Essays (trans. J.M. Cohen). Penguin Books, Harmondsworth, UK
Montaigne, M. de. 1603 (1998). Florio's translation of Montaigne's essays. B. R. Schneider (ed.), Renascence Editions, University of Oregon
Moon, A.M. and M.R. Capecchi. 2000. Fgf8 is required for outgrowth and patterning of the limbs. Nature Genetics 26: 455-459
Morin, A. 1996. La teratologic de Geoffroy Saint-Hilaire à nos jours. Bulletin de l'Association des Anatomistes 80: 17-31
Morishima, A. et al. 1995. Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens. Journal of clinical endocrinology and metabolism 80: 3689-3698
Mortlock, D.P. and J.W. Innis. 1997. Mutation of Hox a-13 in hand-foot-genital syndrome. Nature Genetics 15: 179-180
Mortlock, D.P. et al. 1996. The molecular basis of hypodactyly (Hd): a deletion in Hox a-13 leads to arrest of digital arch formation. Nature Genetics 13: 284-288
Moskovitz, E. 1987. By the grace of the devil. Rotem, Ramat-Gan, Israel
Muenke M. and P.A. Beachy 2000. Genetics of ventral forebrain development and holoprosencephaly. Current Opinion in Genetics and Development 10: 262-269
Mundlos, S. 1999. Cleidocranial dysplasia: clinical and molecular genetics. Journal of Medical Genetics 36: 177-182
Mundlos, S. et al.1997. Mutations involving the transcription factor CBFAi cause cleiodocranial dysplasia. Cell 89: 773-779
Muragaki, Y. et al. 1996. Altered growth and branching patters in synpolydactyly caused by mutations in Hoxd-13. Science 272: 548-551
Mya-Tu, M. et al. 1962. Tarong pygmies in North Burma. Nature 195: 131-132
Mya-Tu, M. et al. 1966. The Tarons in Burma. Burma Medical Research Institute, Rangoon. Special Report Series No.1
Nanni, L. et al. 1999. The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly. Human Molecular Genetics 8: 2479-2488
Nanni, L. et al. 2001. SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature. Journal of Medical Genetics 102: 1-10, 2001
Naski, M.C. et al. 1996. Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia. Nature Genetics 13: 233-237
Naski, M.C. et al. 1998. Repression of hedgehog signalling and BMP4 expression in growth plate cartilage by fibroblast growth factor receptor 3. Development 125: 4977-4988
Naudin ten Cate L., C. Vermeij-Keers, D.A. Smit, T.W. Cohen-Overbeek, K.B. Gerssen-Schoorl, T. Dijkhuisen. 1995. intracranial teratoma with multiple fetuses. Pre- and post-natal appearance. Human Pathology 26: 804-807
Neaves, W.B. et al. 1980. Sexual dimorphism of the phallus in spotted hyena (Crocuta crocuta). Journal of Reproduction and Fertility 59: 509-513
Needham, J. 1959. A history of embryology. Cambridge University Press, Cambridge, UK
Netter, A. et al. 1958. Le testicule feminisant. Annales d'endocrinologie 9: 994-1014
Neubert, R. et al. 1999. Developmental model for thalidomide action. Nature 400: 419-420
Newbery, H.J. and C.M. Abbott. 2002. Of mice, men and motor neurons. Trends in Molecular Medicine 8: 88-92
Niccoli, O. 1990. People and prophecy in Renaissance Italy, (trans. L. G. Cochrane.) Princeton University Press, Princeton
Niswander, L. et al. 1993. FGF-4 replaces the apical ectodermal ridge and directs outgrowth and patterning of the limb. Cell 75: 579-587
Nonaka, S. et al. 1998. Randomisation of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein. Cell 95: 839-847
Noramly, S. and B.A. Morgan. 1998. BMPs mediate lateral inhibition at successive stages in feather tract development. Development 125: 3775-3787
O'Connell, H.E. et al. 1998. Anatomical relationship between urethra and clitoris. Journal of Urology 159: 1892-1897
Olbrich, H. et al. 2002. Mutations in DNAH5 cause primary ciliary dyskinesia and randomisation of left-right asymmetry. Nature Genetics 30: 143-144
Olsen, B.R. et al. 2000. Bone development. Annual Reviews of Cell and Developmental Biology 16: 191-220
On-line Mendelian Inheritance in Man. 2000. OMIM™. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University, Baltimore, MD, and National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD
Oosterhout, van C. et al. 2003. Inbreeding depression and genetic load of sexually selected traits: how the guppy lost its spots. Journal of Evolutionary Biology 16: 273-281
Oostra, R.-J. et al. 1998a. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. I: Syndromes with multiple congenital anomalies. American Journal of Medical Genetics 77: 100-115
Oostra, R.-J. et al. 1998b. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. II: Skeletal Dysplasias. American Journal of Medical Genetics 7 7: 116-134
Oostra, R.-J. et al. 1998c. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. Ill: Primary field defects, sequences and other complex anomalies. American Journal of Medical Genetics 80: 46-59
Oostra, R.-J. et al. i998d. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. IV: Closure defects of the neural tube. American Journal of Medical Genetics 80: 60-73
Oostra, R.-J. et al. 19986. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. V: Conjoined and acardiac twins. American Journal of Medical Genetics 80: 74-89
Oro, A.E. and M.P. Scott. 1998. Splitting hairs: dissecting roles of signaling systems in epidermal development. Cell 95: 575-578
Orr, H.T. 2000. A proposed mechanism of ALS fails the test in vivo. Nature Neuroscience 5: 287-288
Ortega-Ortiz, J.G. and B. Villa-Ramirez. 2000. Polydactyly and other features of the manus of the vaquita, Phocoena sinus. Marine Mammal Science 16: 277-286
Pare, A. 1573 (1971). Des monstres. J. Ceard (ed.) Droz, Geneva
Pare, A. 1573 (1982). On monsters and marvels (trans. J. L. Pallister) Chicago University Press, Chicago
Park, K. and L. Daston. 1981. Unnatural conceptions: the study of monsters in sixteenth and seventeenth century France and England. Past and Present 92: 20-54
Parkes, T.L. et al. 1998. Extension of Drosophila lifespan by over expression of human SOD1 in motorneurons. Nature Genetics 19: 171-174
Partridge, L. and D. Gems. 2002. Mechanisms of ageing: public or private? Nature Reviews Genetics 3: 165-175
Patronek, G.J. et al. 1997. Comparative longevity of pet dogs and humans: implications for gerontology research. Journal of Gerontology 52A: B171-178
Pearson, K. et al. 1913. A monograph on albinism in man. 3 V. text; 3 V. plates. Draper's company research memoirs, Biometric series X. Dulau & Co. London
Pearson, K. 1908. On the inheritance of the deformity known as split-foot or lobster claw. Biometrika 6: 69-79
Pearson, K. 1913. Notes on the Honduras piebald. Biometrika 9: 330-331
Perrett, D.I. et al. 1994. Facial shape and judgments of female attractiveness. Nature 368: 239-242
Perriton, C. et al. 2002. Sonic hedgehog signalling from the urethral epithelium controls external genital development Developmental Biology 247: 26-46
Piccolo, S. et al. 1996. Dorsoventral patterning in Xenopus: inhibition of ventral signals by direct binding of Chord in to BMP-4. Cell 86: 589-598
Pinto-Correa, C. 1997. The ovary of Eve: egg and sperm and preformationism. Chicago University Press, Chicago
Pletcher, S.D. et al. 2002. Genome-wide transcript profiles in aging and calorically restricted Drosophila melanogaster. Current Biology 30: 712-723
Posel, D. 2001. Race as common sense: racial classification in twentieth century South Africa. African Studies Review 44: 87-113
Posner, G. L. and J. Ware. 1986. Mengele: the complete story. Futura, London
Power, C. and S. Matthews. 1997. Origins of health inequalities in a national population sample. Lancet 350: 1584-1589
Qu, S. et al. 1998. Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly. Development. 125: 2711-2721
Quance, E. 1977. Alexander Graham Bell, human inheritance, and the eugenics movement. Research Bulletin of the National Historic Parks and Sites Branch, Parks Canada. No. 62
Quigley, C.A. et al. 1992. Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status. Journal of Clinical Endocrinology and Metabolism 74: 932-933
Ramesar, R.S. et al. 1996. Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity. Journal of Medical Genetics 33: 511-514
Ramirez-Solis et al. 1993. Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cerivical rudiment and defects in the closure of the sternal rudiments. Cell 73: 279-294
Rana, B.K. et al. 1999. High polymorphism at the human melanocortin 1 receptor locus. Genetics 151: 1547-1557
Rancourt et al. 1995. Genetic interaction between Hoxb-5 and Hoxb-6 is revealed by nonallelic noncomplementation. Genes and Development 9: 108-122
Reaume, A.G. et al. 1996. Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury. Nature Genetics 13: 43-47
Reed, Т.Е. and J.V. Neel. 1959. Huntington's chorea in Michigan. American Journal of Human Genetics 11: 107-635
Reeves, R.H. et al. 2001. Too much of a good thing: mechanisms of gene action in Down syndrome. Trends in Genetics 17: 83-241
Reichert, H. and A. Simeone. 2001. Developmental genetic evidence for a monophyletic origin of the bilaterian brain. Philosophical Transactions of the Royal Society В 356: 1533-1544
Reynolds, A.J. et al. 1999. Trans-gender induction of hair follicles. Nature 402: 46-47
Ricklefs, R.E. and C.E. Finch. 1995. Ageing: a natural history. Scientific American, N.Y.
Riddle, R.D. et al. 1993. Sonic hedgehog mediates the Polarizing Activity of the ZPA. Cell 75: 1401-1416
Robbins, L.S. et al. 1993. Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell 72: 827-834
Roberts, R.S. 1974. The making of a Rhodesian myth. Rhodesian History 5: 89-91
Robins, A.H. 1991. Biological perspectives on human pigmentation. Cambridge University Press, Cambridge, UK
Rodriguez, J.M. 1870. Descripcion de un monstruo cuadruple, nacido en Durango el ano de 1860. Gaceta Medica de Mexico 5: 33-48
Roessler, E. et al. 1996. Mutations in the human sonic hedgehog gene cause holoprosencephaly. Nature Genetics 14: 357-360
Root, A. 1998. Editorial: does growth hormone have a role in the management of children with nongrowth hormone deficient short stature and intrauterine growth retardation? Journal of Clinical Endocrinology and Metabolism 83: 1067-1069
Rose, M.R. 1984. Laboratory evolution of postponed senescence in Drosophila melanogaster. Evolution 38: 1004-1010
Rose, M.R. 1991. Evolutionary biology of ageing. Oxford University Press, N.Y.
Rosen, D.R. et al. 1993. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362: 59-62
Rosenbaum, S. et al. 1985. A survey of heights and weights of adults in Great Britain. Annals of Human Biology 12: 115-127
Rosenbloom, A.L. and J.G. Guevara-Aguirre. 1998. Lessons from the genetics of Laron syndrome. Trends in Endocrinology and Metabolism 9: 27-83
Rosenburg, N.A. et al. 2002. Genetic structure of human populations. Science 298: 2381-2385
Rosenfeld, R.G. et al. 1994. Growth hormone (GH) insensitivity due to primary GH deficiency. Endocrine Reviews 15: 369-390
Rousseau, F. et al. 1994. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature 371: 252-254
Rousseau, F. et al. 1995. Stop codon FGFR3 mutations in thanatophoric dwarfism type 1. Nature Genetics 10: 11-12
Rubinsztein, D.C. 2002. Lessons from animal models of Huntington's disease. Trends in Genetics 18: 202-209
Rudolph, K.L. et al. 1999. Longevity, stress response, and cancer in aging telomerase-deficient mice. Cell: 96: 701-712
Russell, A.J. et al. 1994. Mutation in the human gene for 3 alpha-hydroxysteroid dehydrogenase type II leading to male pseudohermaphroditism without salt loss. Journal of Molecular Endocrinology 12: 225-237
Sadler, T.W. 2000. Longman's medical embryology (8th ed.) Lippincott Williams & Wilkins, Philadelphia
Saegusa, H. et al. 1996. Targeted disruption of HoxC-4 locus results in axial skeleton homeosis and malformation of the xiphoid process. Developmental Biology 174: 55-64
Saint-Ange, M. 1830. Journal hebdomaidaire de médécine 6: 42-49
Sakai, Y. et al. 2001. The retinoic acid-inactivating enzyme CYP26 is essential for establishing an uneven distribution of retinoic acid along the anterio-posterior axis within the mouse embryo. Genes and Development 15: 213-225
Samaras, T. and H. Elrick. 1999. Height, body size and longevity. Acta Medica Okayama 53: 149-169
Silmaras, T. et al. 1999. Height, health and growth hormone. Acta Paediatrica 88: 602-609
Sandberg, D.E. et al. 1994. Short stature: a psychosocial burden requiring growth hormone therapy? Pediatrics 94: 832-839
Sato, N. et al. 1999. Induction of the hair growth phase in postnatal mice by localized transient expression of sonic hedgehog. Journal of Clinical Investigation 104: 855-864
Saunders, J.W. 1948. The proximo-distal sequence of origin of the parts of the chick wing, and the role of the ectoderm. Journal of Experimental Zoology 108: 363-403
Saunders, J.W. and M.T. Gasseling. 1968. Ectodermal-mesenchymal interactions in the origin of limb symmetry, in R. Fleischmajer and R.F. Billingham (eds). Epithelial-Mesenchymal interactions pp. 78-97 Williams and Wilkins, Baltimore
Scarry, E. 2000. On beauty and being just. Duckworth, London
Schachter, F. et al. 1994. Genetic associations with human longevity at the APOE and ACE loci. Nature Genetics 6: 29-32
Schatz, E. 1901. Die Griechischen Götter und die Menschlichen Missgeburten. J.F. Bergmann Verlag, Wiesbaden (reprint 1969, Editions Rodopi, Amsterdam
Schebesta, P. 1952. Die Negrito Asiens 3 vols. Vienna
Schnaas, G. 1974. ElPerro Pelon: mito, fantasia уbiologia. Gaceta medica de mexico 108: 393-400
Schnitzer, E. 1888. Emin Pasha in central Africa. Schweinfurth, G., Ratzel, F. Felkin, RW. Hartlatier, G. (eds) Philip and Son. London
Schweinfurth, G. 1878. The heart of Africa (trans. E. E. Frewer). 3rd edition. Sampson Low, Marston, Searle & Rivington, London
Segrave, K. 1996. Baldness, a social history. McFarland & Co. Jefferson, NC, USA
Semonin, O. et al. 2001. Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva. American Journal of Medical Genetics 102: 314-317
Serres, E. 1832. Recherches d'anatomie transcendante et pathologique. Théorie des formations et déformations organiques, appliquée à I'anatomie de Ritta-Christina, et de la duplicité monstrueuse. J.B. Balliere, Paris
Seward, G.R. 1992. The Elephant Man. British Dental Association, London
Shriver, M.D. et al. 2003. Skin pigmentation, biogeographical ancestry and admixture mapping. Human Genetics 112: 387-399
Sgro, C. and L. Partridge. 1999. A delayed wave of death from reproduction in Drosophila. Science 286: 2521-2524
Sharpe, P. 2001. Fish scale development: hair today, teeth and scales yesterday? Current Biology II: R751-752
Sharpe, R.M. 1998. The roles of estrogen in the male. Trends in Endocrinology and Metabolism 9: 371-377
Shay, J.W. and W.E. Wright. 2000. Hayflick, his limit, and cellular ageing. Nature Reviews Molecular Cell Biology I: 72-75
Shea, B.T. and A.M. Gomez. 1988. Tooth scaling and evolutionary dwarfism: an investigation of allometry in human pygmies. American Journal of Physical Anthropology 77: 117-132
Shea, B.T. 1989. Heterochrony in human evolution: the case for neoteny reconsidered. Yearbook of Physical Anthropology 32: 69-101
Shea, B.T. and R.C. Bailey. 1986. Allometry and adaptation of body proportions and stature in African pygmies. American Journal of Physical Anthropology 100: 311-340
Shiels, P.G. et al. 1999. Analysis of telomere lengths in cloned sheep. Nature 399: 317
Shozu; M. et al. 1991. A new cause of female pseudohermaphroditism: placental aromatase deficiency. Journal of Clinical Endocrinology and Metabolism 72: 560-566.
Shubin, N.H. and P. Alberch. 1986. A morphogenetic approach to the organization of the tetrapod limb. Evolutionary Biology 20: 319-387
Shubin, N.H. et al. 1997. Fossils, genes and the evolution of animal limbs. Nature 388: 639-648
Sidow, A. et al. 1999. A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant. Nature Genetics 23: 104-107
Siebold, von C.T. 1878. Die Haarige familie von Ambras. Archiv für Anthropolgie 10: 253-260
Silventoinen, K. et al. 1999. Social background, adult body-height and health. International Journal of Epidemiology 28: 911-918
Siminoski, K. and J. Bain. 1993. The relationship among height; penile length and foot size. Annals of Sex Research 6: 231-235
Sinclair, A.H. et al. 1990. A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature 346: 240-244
Slijper, E.J. 1942. Biologic-anatomical investigations on the bipedal gait and upright posture in mammals, with special reference to a little goat, born without forelegs. I., II. Proceedings Koninklijke Nederlandse Academie van Wetenschap 45: 288-295; 407-415
Smith, E.P. et al. 1994. Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man. New England Journal of Medicine 331: 1056-1061
Smith, R. et al. 1998. Melanocortin 1 receptor variants in an Irish population. Journal of Investigative Dermatology III: 119-122
Sordino, P. et al. 1995. Hoxgene expression in teleostfins and the origin of vertebrate digits. Nature 375: 678-681
Sornson, M.W. et al. 1996. Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism. Nature. 384: 327-332
Sparks, C.S. and R.L. Jantz. 2002. A reassessment of human cranial plasticity: Boas revisited. Proceeding of the National Academy of Sciences USA 99: 14636-14639
Spemann, H. and H. Mangold. 1924. Über die induktion von Embryonalanlagen durch Implantation artfremder Organisatoren. Archiv für mikroskopische Anatomie und Entwicklungsmechanik 100: 599-638
Spencer, R. 2000a. Theoretical and analytical embryology of conjoined twins: Part 1: Embryogenesis. Clinical Anatomy 13: 36-53
Spencer, R. 2000b. Theoretical and analytical embryology of conjoined twins: Part 2: Adjustments to union. Clinical Anatomy 13: 97-20
Spencer, R. 2001. Theoretical and analytical embryology of conjoined twins: Part 3: External, internal (fetuses in fetu and teratomas) and detached (Acardiacs). Clinical Anatomy 14: 428-444
Steinman, G. 2001a. Mechanisms of twinning. I. Effect of environmental diversity on genetic expression in monozygotic multifetal pregnancies. The Journal of Reproductive Medicine 46: 467-472
Steinman, G. 2001b. Laterality and intercellular bonding in monozygotic twinning. The Journal of Reproductive Medicine 46: 473-479
Stephens, J.C. et al. 2001. Haplotype variation and linkage disequilibrium in 313 human genes. Science 293: 489-493
Stephens, T.D. et al. 2000. Mechanism of action in thalidomide teratogenesis. Biochemical Pharmacology 59: 1489-1499
Stevens, G. et al. 1997. Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation. Human Genetics 99: 523-527
Stratakis, C.A. et al. 1998. The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P 450 aromatase gene transcription. Journal of Clinical Endocrinology and Metabolism 83: 1348-1357
Sturm, R.A. et al. 1998. Human pigmentation genetics: the difference is only skin deep. Trends in Genetics 20: 712-721
Subramaniam, J.R. et al. 2002. Mutant SODI causes motor neuron disease independent of copper chaperone-mediated copper loading. Nature Neuroscience 5: 301-307
Sun, X. et al. 2002. Functions of FGF signalling from the apical ectodermal ridge in limb development. Nature 418: 501-508
Sutton, J.B. 1890. Evolution and disease. Walter Scott, London
Szabo, G. et al. 1969. Racial differences in the fate of the melanosomes. Nature 222: 1081-1082
Tabin, C. 1998. A developmental model for thalidomide defects. Nature 396: 322-323
Tabin, C. 1999. Developmental model for thalidomide action – reply. Nature 400: 420
Takahashi, E. Secular trend in milk consumption and growth in Japan. Human Biology 56: 427-437
Ta-Mei, W. et al. 1982. Craniopagus parasiticus: a case report of a parasitic head protruding from the right side of the face. British Journal of Plastic Surgery 35: 304-311
Tang, D.G. et al. 2001. Lack of replicative senesence in cultured rat oligodendrocyte precusor cells. Science 291: 868-871
Tanner, J.M. 1981. A history of the study of human growth. Cambridge University Press, Cambridge, UK
Tanner, J.M. 1984. Foetus into man. (Revised ed.) Harvard University Press, Cambridge, Mass.
Tassabehji, M. et al. 1992. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 355: 635-636
Tatsumi, K. et al. 1992. Cretinism with combined hormone deficiency caused by a mutation in the pit-1 gene. Nature Genetics 1: 56-58
Taussig, H.B. 1988. Evolutionary origin of cardiac malformations. Journal of the American College of Cardiology 12: 1079-1086
Tavormina, P.L. et al. 1995. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nature Genetics 9: 321-328
Thadini, K.I. 1934. The toothless men of Sind. Journal of Heredity 26: 65-66
Thangaraj, K. 2003. Genetic affinities of the Andaman Islanders, a vanishing human populations. Current Biology 13: 86-93
Thiery, M. and H. Houtzager. 1997. Der Vrouwen Vrouwlijcheit. Erasmus, Rotterdam
Thompson, A.A. and L.T. Nguyen. 2000. Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation. Nature Genetics 26: 397-398
Thompson, C.J.S. 1930 (1994) The history and lore of freaks. Senate. London
Thornhill, R. and S.W. Gangestad. 1999. Facial attractiveness. Trends in Cognitive Science 3: 452-460
Tibbies, J.A.R and M.M. Cohen. 1986. The Proteus syndrome: the Elephant Man diagnosed. British Medical Journal 293: 683-685
Tickle, C. et al. 1975. Positional signalling and specification of digits in chick limb morphogenesis. Nature 20: 199-202
Tietze-Conrat, E. 1957. Dwarfs and jesters in art. Phaidon. London
Tjalma, R.A. 1966. Canine bone sarcoma: estimation of relative risk as function of body size. Journal of the National Cancer Institute. 36: 1137-1150
Toda, K. et al. 1972. Racial differences in melanosomes. Nature New Biology 236: 143-145
Ton, C.T. et al. 1991. Positional cloning and characterization of a Paired Box- and Homeobox-containing gene from the Aniridia region. Cell 67: 1059-1074
Touchefeu-Meynier, О. 1992. Kyklops, Kyklopes. text pp.154-9; plates pp.69-75 in Lexicon iconographicum mythologiae classical: VI: 1 (text); 2 (plates)
Townsend, P. et al. 1992. Inequalities in health. Penguin Books, Harmondsworth, UK
Trotter, M. 1928. Hair growth and shaving. Anatomipal Record 37: 373-379
Tsukui, T. et al. 1999. Multiple left-right asymmetry defects in Shh-/-mutant mice unveil a convergence of the Shh and retinoic acid pathways in the control of Lefty-1. Proceedings of the National Academy of Sciences, USA. 96: 11376-11381
Twitty, V.C. 1966. Of scientists and salamanders. W.H. Freeman and Co., San Francisco
Twitty, V.C. and J.L. Schwind. 1931. The growth of eyes and limbs transplanted heteroplastically between two species of Amblystoma (sic). Journal of Experimental Zoology 59: 61-86
Tyson, E. 1699 (1966). A philological essay concerning the pygmies of the ancients. B. Windle (ed.). David Nutt, London
Unthan, C.H. 1935. The armless fiddler: a pediscript. George Allen & Unwin, London
Valenzano, M. et al. 1999. Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. Human Reproductive Update 5: 82-86
Valverde, P. et al. 1995. Variants of the melanocyte stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nature Genetics II: 328-330
Vassart, G. 2000. TSH receptor mutations and diseases Ch. 16a. The Thyroid and Its Diseases:
Vieille-Grosjean, I. et al. 1997. Branchial Hox gene expression and human craniofaciall development. Developmental Biology 183: 49-60
Viljoen, D.L. and P. Beighton. 1984. The split-hand and split-foot anomaly in a central African Negro population. American Journal of Medical Genetics 19: 545-552
Viljoen, D.L. and S.H. Kidson. 1990. Mirror-polydactlyly – pathogenesis based on a morphogen gradient theory. American Journal of Medical Genetics 35: 229-235
Voss, J.W. and M.G. Rosenfeld. 1992. Anterior pituitary development. Cell 70: 527-530
Vrolik, W. 1834. Over den aard en oorsprong der cyclopie. Niewe verhandelingen der Eerste Klasse van het Koninklijk Nederland Instituut. 5: 25112
Vrolik, W. 1844-49. Tabulae ad illustrandam embryogenesin hominis et mammalium tarn naturalem quam abnormem. Amsterdam, London
Waaler, H.T. 1984. Height, weight and mortality: the Norwegian experience. Acta Medica Scandinavia Supplement 679: 1-56
Walton, M.T. et al. 1993. Of monsters and prodigies: the interpretation of birth defects in the sixteenth century. American Journal of Medical Genetics 47: 7-13
Watanabe, A. et al. 1998. Epistatic relationship between Waardenburg syndrome genes MITF and PAX3. Nature Genetics 18: 283-286
Weber, G. 1995-99. Lonely islands: the Andamanese. The Andaman Association, Switzerland:
Weinstein, B.S. and D. Ciszek. 2002. The reserve-capacity hypothesis: evolutionary origins and modern implications of the trade-off between tumor-suppression and tissue repair: Experimental Gerontology 37: 615-627
Westendorp, R.G.J, and T.B.L. Kirkwood. 1998. Human longevity and the cost of reproductive success. Nature 396: 743-746
Wilkie, A.O. et al. 1995. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genetics 9: 165-172
Williams, D. 1996. Deformed discourse. The function of the monstrous in medieval thought. University of Exeter Press
Williams, G.C. 1957. Pleiotropy, natural selection, and the evolution of senesence. Evolution II: 398-411
Williams, G.R. 1998. Thyroid hormone action on cartilage and bone: interactions with other hormones at the epiphyseal plate and effects on linear growth. Journal of Endocrinology 157: 391-403
Williamson, S. and R. Nowak. 1998. The truth about women. New Scientist. 159: 34-35
Willier, B.H. and J.M. Oppenheimer. 1964. Foundations of experimental embryology. Prentice-Hall, N.J.
Wilmoth, J.R. et al. 2000a. Demography of longevity: past, present, arid future trends. Experimental Gerontology 35: 1111-1129
Wilmoth, J.R. et al. 2000b. Increase of maximum life-span in Sweden, 1861-1999. Science 289: 2366-2386
Wilmut, I. 2002. Are there any normal cloned animals? Nature Medicine 8: 215-216
Wilmut, I. et al. 1997. Viable offspring derived from fetal and adult mammalian cells. Nature 385: 810-813
Wilson, D. 1993. Signs and portents: monstrous births from the Middle Ages to the Enlightenment. Routledge, London
Wilson, J.D. and C. Roehrborn. 1999. Long term consequences of castration in men: lessons from the Skoptzy and the Eunchs of the Chinese and Ottoman Courts. Journal of Clinical Endocrinology and Metabolism 84: 4324-4331
Winter, R.M. 1996. What's in a face? Nature Genetics 12: 124-129
Winter, R.M. and D. Donnai. 1989. A possible human homologue for the mouse mutant disorganisation. Journal of Medical Genetics 26: 417-420
Wittkower, R. 1942. Marvels of the East. Journal of the Warburg and Courtauld Institutes 5: 159-197
Wolpert, L. 1971. Positional information and pattern formation. Developmental Biology 6: 183-224
Woolf, C.M. and F.C. Dukepoo. 1969. Hopi Indians, inbreeding, and albinism. Science 164: 30-37
Worden, G. 2002. Mutter Museum. Blast Books, N.Y.
Wright, S. 1935. A mutation of the guinea-pig, tending to restore the pentadactyl foot when heterozygous, producing a monstrosity when heterozygous. Genetics 20: 84-107
Wu, W. et al. 1998. Mutations in prop-1 cause familial combined pituitary hormone deficiency. Nature Genetics 18: 147-149
Yang, A. et al. 1999. рбзis essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature 398: 714-718
Yang, Y. et al.1997. Relationship between dose, distance and time in sonic hedgehog mediated regulation of anteroposterior polarity in the chick limb. Development 124: 4393-4404
Yu, C.E. et al. 1989. Positional cloning of the Werner's syndrome gene. Science 272: 258-262
Yule, H. 1858. A narrative of the mission sent by the Governor-General of India to the court of Ava in 1855. Bell, N.Y.
Zeikany, J. et al. 1997. Regulation of number and size of digits by posterior Hox genes: A dose dependent mechanism with potential evolutionary implications. Proceeding of the National Academy of Sciences, USA 94: 1395-13700
Zapperi. R. 1995. Ein Haarmensch auf einem Gamalde von Agostino Carracci. in Hagner, M. (ed.) Der falsche Korper: Bietriige zu einer Geschichte der Monstrositaten. Wallstein, Gottingen
Zekraoui, L. et al. 1997. High frequency of the apolipoprotein ε4 allele in African pygmies and most of the African populations in sub-Saharan Africa. Human Biology 69: 575-581
Zeng, X. et al. 2001. A freely diffusible form of sonic hedgehog mediates long-range signalling. Nature 411: 716-720
Zguricas, J. et al. 1999. Clinical and genetics studies on 12 preaxial polydactlyly families and refinement of the localization of the gene responsible to a1.9 cM region on chromosome 7q35. Journal of Medical Genetics 36: 32-40
Zhou, X.-P. et al. 2000. Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lowerlimb asymmetry, arteriovenous malformations and lipomatosis. Human Molecular Genetics 19: 765-768
Zhou, X.-P. et al. 2001. Association of germline mutation in the PTEN tumor suppressor gene and Proteus and Proteus-like syndromes. Lancet 358: 210-211
Zimmerman, L.B. et al. 1996. The Spemann organizer signal noggin binds and inactivates Bone morphogenetic protein-4. Cell 86: 599-606
Zou, H. and L. Niswander. 1996. Requirement for BMP signalling in interdigital apoptosis and scale formation. Science 272: 738-741

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