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. Uber die induktion von Embryonalanlagen durch Implantation artfremder Organisatoren. Archiv fur 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
