Skip to main content Accessibility help

Genetic counselling*

  • B. C. Clare Davison (a1)


  • An abstract is not available for this content so a preview has been provided below. Please use the Get access link above for information on how to access this content.



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

Genetic counselling*

  • B. C. Clare Davison (a1)


Full text views

Total number of HTML views: 0
Total number of PDF views: 0 *
Loading metrics...

Abstract views

Total abstract views: 0 *
Loading metrics...

* Views captured on Cambridge Core between <date>. This data will be updated every 24 hours.

Usage data cannot currently be displayed.