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.Rand 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