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