eighteenth century. Reaktion, London
Birkett, J. 1858. Congential, supernumerary and imperfectly developed auricles on the sides of the neck. Transactions of the Pathological Society of London 9: 448-449
Bittles, A.H. 2001. Consaguinity and its relevance to clinical genetics Clinical Genetics 60: 89-90
Blair, H.C. 1998. How the osteoclast degrades bone. Bioessays 20: 837-846
Blanchard, R. 1907. Nouvelles observations sur les negres pies. Geoffroy Satin-Hilaire a Lisbonne. Bulletin de la Societe Franсaise d'histoire de la medecine 6: 111-135
Blasco, M.A. et al. 1997. Telomere shortening and tumor formation by mouse cells lacking telomerase RNA. Cell 91: 25-34
Boaistuau, P. 1560 (2000) Histoires prodigieuses, Facsimile of Wellcome MS 136. (S. Bamforth ed.) Franco Maria Ricci, Milan
Boardman, J. 1997a. Pan in text pp. 923-941; plate pp. 612-636 in Lexicon iconographicum mythologiae classicae: VIII: 1 (text); 2 (Plates)
Boardman, J. 1997b. The great god Pan. Thames and Hudson, London
Boas, F. 1912. Changes in bodily form of descendants of immigrants. American Anthropologist 14: 530-562
Bodnar, A.G. et al. 1998. Extension of life-span by introduction of telomerase into normal human cell. Science 279: 349-351
Bogin, B. 1999. Patterns of human growth, 2nd ed. Cambridge University Press, Cambridge. UK
Bonaventure, J. et al. 1996. Common mutations in the Fibroblast Growth Factor Receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia and thanatophoric dwarfism. American journal of Medical Genetics 63: 148-154
Bondeson, J. 1997. A cabinet of medical curiosities. Tauris, London
Bondeson, J. 2000. The two-headed boy and other medical marvels. Cornell University Press, Ithaca. N.Y.
Bondeson, J. and A.E.W. Miles. 1996. The hairy family of Burma: a four generation pedigree of congenital hypertrichosis lanuginosa. Journal of the Royal Society of Medicine 89: 403-408
Bornstein, P.E. and R.R. Peterson. 1966. Numerical variation in the presacral vertebral column in three population groups. American Journal of Physical Anthropology 25: 139-146
Boruwlaski, J. 1792. The Memoirs of the celebrated dwarf Joseph Boruwlaski, A Polish gentleman containing a faithful and curious account of his birth, education, marriage, travels and voyages, (trans. S. Freeman) 2nd ed. J. Thompson. Birmingham
Boulet and Capecchi. 1996. Targeted disruption of Hoxc-4 causes esophageal defects and vertebral transformation. Developmental Biology 177: 232- 249
Boyd, W.C. 1955. Genetics and the races of man. Little, Brown and Co., Boston
Brandtt A. 1897. Ueberdiesogenannten Hundemenschen, beziehungsweise uber Hypertrichosis universalis. Biologische Zentralblatt 17: 161-179
Broberg, G. 1983. Homo sapiens. Linnaeus' classification of man. in T. Frangsmyr, (ed.) Linnaeus: the man and his work. University of California Press, Berkley
Brockes, J.P. 1998. Regeneration and cancer. Biochimica et biophysica acta. 1377 M1-M11
Brown-Borg, H.M. et al. 1996. Dwarf mice and ageing process. Nature 384: 33
Browne, T. 1904. The works of Thomas Browne. C. Sayle (ed.) Grant Richards, London
Brueckner, M. 2001. Cilia propel the embryo in the right direction. American Journal of Medical Genetics 101: 339-344
Brunet, L.J. et al. 1998. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. Science 280: 1455-1457
Brunkow, M.E. et al. 2001. Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. American Journal of Human Genetics 68: 577-589
Bruyn, G.W. and L.N. Went. 1986. Huntington's Chorea, in Vinken, G. W. et al. (eds.) Extrapyramidal disorders: handbook of clinical neurology 49: 267-273
Buffon, G.L. 1777. Histoire naturelle generale et particuliere. Imprimerie Royale, Paris
Burn, J. and T. Strachan. 1995. Human embryo use in developmental research. Nature Genetics 11: 3-6
Callahan, C.A. and A.E. Oro. 2001. Monstrous attempts at adnexogenesis: regulating hair follicle progenitors through sonic hedgehog signalling. Current Opinion in Genetics and Development 11: 541-546
Cargill, M. et al. 1999. Characterisation of single-nucleotidepolymorphisms in coding regions of human genes. Nature Genetics 22: 231-238
Carpenter, E.M. et al. 1993. Loss of Hox-Al (Hox-1.6) function results in the reorganisation of the murine hindbrain. Development 118: 1063-1075
Casey, B. and B.P. Hackett. 2000. Left-right axis malformations in man and mouse. Current Opinon in Genetics and Development 10: 257-261
Cavalli-Sforza, L.L. 1986. The African pygmies. Academic Press, N.Y.
Cavelaars, A.E.J.M. et al. 2000. Persistent variations in average height between countries and between socio-economic groups: an overview of 10 European countries Annals of Human Biology 27: 407-421
Celli, J. et at. 1999. Heterozygous germline mutations in the P53 homolog p63 are the cause of EEC syndrome. Cell 99: 143-151
Chapman, T. and L. Partridge. 1996. Female fitness in Drosophila melanogaster: an interaction between the effect of nutrition and of encounter rates with males. Proceedings of the Royal Society, London Series ВBiological Sciences 263: 755-759
Charlesworth, B. 1996. Evolution of senescence: Alzheimer's disease and evolution. Current Biology 6: 20-22
Chen, L. et al. 2001. A Ser{j65)->Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates ihh / PTHrP signals and causes severe achondroplasia. Human Molecular Genetics 10: 457-465.
Chen, Y. et al. 2000. Conservation of early odontogenetic signaling pathways in Aves. Proceedings of the National Academy, USA 97: 10044-10049
Chiang, C. et at. 1996. Cyclopia and defective axial patterning in mice lacking sonic hedgehog gene function. Nature 383: 407-412
Chiang, C. et al. 2001. Manifestation of the limb prepattern: limb
