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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: 284–93

Martin, E. 1880. Histoire des monstres. C. Reinwald, Paris

Martin, G. and J. Oshima. 2000. Lessons from human progeroid syndromes. Nature 408: 263–6

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: 315–24

Mathon, N.F. et al. 2001. Lack of replicative sensecence in normal rodent glia. Science 291: 872–5

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 der czwo grewlichï Figuren, etc.]

Merimee, T.J. et al. 1981. Dwarfism in the pygmy. New England Journal of Medicine 305: 965–8

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: 906–11

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: 403–6

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: 708–13

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: 366–9

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: 455–9

Morin, A. 1996. La teratologic de Geoffroy Saint-Hilaire á 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: 3689–98

Mortlock, D.P. and J.W. Innis. 1997. Mutation of Hox a-13 in hand-foot-genital syndrome. Nature Genetics 15: 179–80

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: 284–8

Moskovitz, E. 1987. By the grace of the devil. Rotem, Ramat-Gan, Israel

Muenke M. and PA. Beachy 2000. Genetics of ventral forebrain development and holoprosencephaly. Current Opinion in Genetics and Development 10: 262–9

Mundlos, S. 1999. Cleidocranial dysplasia: clinical and molecular genetics. Journal of Medical Genetics 36: 177–82

Mundlos, S. et al. 1997. Mutations involving the transcription factor CBFAi cause cleiodocranial dysplasia. Cell 89: 773–9

Muragaki, Y. et al. 1996. Altered growth and branching patters in synpoly-dactyly caused by mutations in Hox d-13. Science 272: 548–51

Mya-Tu, M. et al. 1962. Tarong pygmies in North Burma. Nature 195: 131–2

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: 2479–88

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 mutaitons causing achondroplasia and thanatophoric dysplasia. Nature Genetics 13: 233–7

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: 4977–88

Naudin ten Gate 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: 804–7

Neaves, W.B. et al. 1980. Sexual dimorphism of the phallus in spotted hyena (Crocuta crocuta). Journal of Reproduction and Fertility 59: 509–13

Needham, J. 1959. A history of embryology. Cambridge University Press, Cambridge, UK

Netter, A. et al. 1958. Le testicule feminisant. Annates d’ endocrinologie 9: 994–1014

Neubert, R. et al. 1999. Developmental model for thalidomide action. Nature 400: 419–20

Newbery, H.J. and CM. 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: 579–87

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: 839–47

Noramly, S. and B.A. Morgan. 1998. BMPs mediate lateral inhibition at successive stages in feather tract development. Development 125: 3775–87

O’Connell, H.E. et al. 1998. Anatomical relationship between urethra and clitoris. Journal of Urology 159: 1892–7

Olbrich, H. et al. 2002. Mutations in DNAH5 cause primary ciliary dyskinesia and randomisation of left–right asymmetry. Nature Genetics 30: 143–4

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. http://www.ncbi.nlm.nih.gov/omim/

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: 273–81