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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: 359–72

Houssay, F. 1937. De la nature, des causes, des differences 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: 4873–84

Huelsken, J. et al. 2001. Beta-catenin controls hair follicle morphogenesis and stem cell differentiation in the skin. Cell 105: 533–45

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: 212–21

Ianakiev, P. et al. 2000. Acheiropodia is caused by a genomic deletion in C7orf2, 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: 1213–15

Imperato-McGinley, J. et al. 1991. A cluster of male pseudohermaphrodites with 5-Alpha-reductase deficiency in Papua New Guinea. Clinical Endocrinology 34: 293–8

Incardona, J.P. 1998. The teratogenic Veratrum alkaloid cyclopamine inhibits sonic hedgehog signal transduction. Development 125: 3553–62

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: 41–8

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: 1613–24

Jackson, W.P.U. 951. Osteo-dental dysplasia (Cleidocranial dysostosis) ‘The Arnold Head’. Acta Medica Scandinavica 139: 293–5

Janin, J. 1829. (1998) Une femme à deux têtes. S. Pestel (ed.) La collection électronique de la Bibliotéque Municipale de Lisieux. http://ourworld.compuserve.com./homepages/bibhhlisieux/

Jarvik, G.P. et al. 1994. Non-mendelian transmission in a human developmental disorder: Split Hand/Split Foot. American Journal of Human Genetics 55: 710–13

Jeannotte, L. et al. (1993) Specification of axial identity in the mouse: role of the Hoxa5 (Hox1. 3) gene. Genes and Development 7: 2085–96

Jenkins, P. 1998. Cancer in acromegaly. Trends in Endocrinology and Metabolism 9: 360–6

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 sexuelle de l’embryon de lapin (Trbisiéme 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, C. 1980. Monstres, démons et merveilles á 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: 707–8

Keith, A. 1911. An inquiry into the nature of the skeletal changes in acromegaly Lancet i: 993–1002

Kenyon, C. et al. 1993. A C. elegans mutant that lives twice as long as wild type. Nature 366: 461–4

Kere, J. et al. 1996. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by a mutation in a novel transmembrane protein. Nature Genetics 13: 409–16

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.F. 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: 993–5

Komori et al. 1997. Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts. Cell 89: 755–64

Kondo, S. et al. 2001. The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor. Current Biology 7: 1201–6

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 a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis. Human Molecular Genetics 9: 2059–63

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: 231–47

Kremer, H. et al. 1995. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinising hormone receptor gene. Nature Genetics 9: 160–4

Krude, H. et al. 1998. Severe early onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nature Genetics 19: 155–7

Kruglyak, L. and D.A. Nickerson. 2001. Variation is the spice of life. Nature Genetics 27: 234–6

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 B or not two B? Journal of the American Academy of Dermatology 11: 921–6

Läära, 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: 408–14

Lahr, M.M. 1996. The evolution of modern human diversity: a study in cranial variation. Cambridge University Press