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Genetic counselling*

Published online by Cambridge University Press:  31 July 2008

B. C. Clare Davison
Affiliation:
25 Bentley Road, Cambridge

Abstract

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Type
Special Article
Copyright
Copyright © Cambridge University Press 1973

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References

Barr, M.L. & Bertram, E.G. (1949) A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis. Nature, Lond. 163, 676.CrossRefGoogle ScholarPubMed
Carter, C.O. & Evans, K.A. (1969) Inheritance of congenital pyloric stenosis. J. med. Genet. 6, 233.CrossRefGoogle ScholarPubMed
Chicago Conference (1966) Standardization of Human Cytogenetics. Birth Defects Original Article Series. Vol. II, No. 2. National Foundation, White Plains, New York.Google Scholar
Court Brown, W.M. (1967) Human Population Cytogenetics. North-Holland Publishing Company, Amsterdam.Google Scholar
Denver Conference (1960) A proposed standard system of nomenclature of human mitotic chromosomes. Ann. hum. Genet. 24, 319.Google Scholar
Edwards, J. (1960) The simulation of Mendelism. Acta genet., Basel, 10, 63.Google ScholarPubMed
Galton, F. (1869) Hereditary Genius. An Enquiry into its Laws and Consequences. Macmillan, London.CrossRefGoogle Scholar
Hamerton, J.L. (1970) Human Cytogenetics. General Cytogenetics. Vol. I. Academic Press, New York and London.Google Scholar
Hamerton, J.L. (1971) Human Cytogenetics. Clinical Cytogenetics. Vol II. Academic Press, New York and London.Google Scholar
Holt, S.B. (1953) Genetics of dermal ridges: bilateral asymmetry in finger ridge counts. Ann. hum. Genet. 18, 211.Google Scholar
Kerr, C.B., Wells, R.S. & Sanger, R. (1964) X-linked ichthyosis and the Xg groups. Lancet, ii, 1369.CrossRefGoogle Scholar
McConnell, R.B. (1966) The Genetics of Gastro-Intestinal Disorders. Oxford University Press, London.Google Scholar
McKusick, V.A. (1971) Mendelian Inheritance in Man. Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes. Third Edition. The Johns Hopkins Press, Baltimore and London.Google Scholar
Pearce, W. G., Sanger, R. & Race, R.R. (1968) Ocular albinism and Xg. Lancet, i, 1282.Google Scholar
Pratt, R.T.C. (1967) The Genetics of Neurological Disorders. Oxford University Press, London.Google Scholar
Renwick, J.H. & Lawler, S.D. (1955) Genetical linkage between the ABO and nail-patella loci. Ann. hum. Genet. 19, 312.CrossRefGoogle ScholarPubMed
Slater, E. & Cowie, V. (1971) The Genetics of Mental Disorders. Oxford University Press, London.Google Scholar
Slatis, H.M., Reis, R.H. & Hoene, R. E. (1958) Consanguineous marriages in the Chicago region. Am. J. hum. Genet. 10, 446.Google ScholarPubMed
Stevenson, A.C. & Davison, B.C.C. (1970) Genetic Counselling. William Heinemann Medical Books, London.Google Scholar
Stevenson, A.C., Davison, B.C.C., Say, B., Ustuoplu, S., Liya, D., Abul-Einen, M. & Toppozada, H.K. (1971) Contribution of fetal/maternal incompatibility to aetiology of preeclamptic toxaemia. Lancet, ii, 1286.CrossRefGoogle Scholar
Tjio, J. H. & Levan, A. (1956) The chromosome number of man. Hereditas, 42, 1.CrossRefGoogle Scholar
Watson, J.D. & Crick, F.H.C. (1953) A structure of deoxyribose nucleic acid. Nature, Lond. 171, 737.CrossRefGoogle ScholarPubMed
Yule, G.U. (1902) Mendel's laws and their probable relation to intra-racial heredity. New Phytol. 1, 193.CrossRefGoogle Scholar