Genetics and Preventive Medicine

Abstract

Get full access to this article

View all access options for this article.

References

Carter, C.O. (1956). Changing patterns in the causes of death at The Hospital for Sick Children Gt. Ormond Str. J., 11, 65.

Böök, J.A. (1955). Heredity Counselling. Medical genetics and counselling practices Eugenics Quarterly , 2, 174.

Neel, J.V. (1951). Some applications of the principles of genetics to the practice of medicine Med. Clinics North Amer., 35, 519.

Sorsby, A. (1950). The Causes of Blindness in England and Wales M.R.C. Memo. No. 24, London.

Fraser, G.R. and Friedmann , A.I. (1967). The Causes of Blindness in Childhood The Johns Hopkins Press, Baltimore, U.S.A.

Fraser, G.R. (1964). Profound Childhood Deafness J. med. Genet., 1, 118.

Stevenson, A.C. (1961). Human Genetics Brit. med. Bull., 17 , 177.

Mckusick, V.A. (1966). Mendelian Inheritance in Man William Heinemann Medical Books, Ltd., London.

Second Report of the W.H.O.

Expert Committee on Human Genetics. Human Genetics and Public Health

Wld. Hlth. Org. Rep., Ser. No. 282.

10.

Medawar, P.B. (1965). Do advances in medicine lead to genetic deterioration? Mayo Clinic Proceedings , 40, 21.

11.

International Commission On Radiological Protection (1964). Pergamon Press, Oxford.

12.

Cohen, M.M. , Marinello, M.J. and Back, N. (1967). Chromosomal damage in human leucocytes induced by lysergic acid diethylamide Science, 155, 1417.

13.

Cohen, M.M. , Hirschhorn, K. , Verbo , S. , Frosch, W.A. and Groeschel , M.M. (1968). The Effect of LSD-25 on the chromosomes of children exposed in utero Pediat. Res., 2, 486.

14.

Zellweger, H. , Mcdonald, J.S. and Abbo, G. (1967). Is lysergic acid diethylamide a teratogen? Lancet , 2, 1066.

15.

Carakushansky, G. , Neu, R.L. and Gardner, L.I. (1969). Lysergic and cannabis as possible teratogens in man Lancet, 1, 150.

16.

Miller, R.W. (1967). Persons with exceptionally high risk of leukaemia Cancer Res., 27, 2420.

17.

Roberts, J.A.F. (1968). Congenital Malformations Postgrad. med. J., 44, 148.

18.

Roberts, J.A.F. (1962). Genetic prognosis Brit. med. J., 1, 587.

19.

Carter, C.O. (1967). Comments on Genetic Counselling Proc. Third Int. Cong. Hum. Genet. , p. 97, Edit. Crow, F. F. and Neel, J. V., Johns Hopkins Press.

20.

Bianco, I. , Montalenti, G. , Silvestroni , E. and Siniscalo, M. (1952). Further data on genetics of microcythaemia or thalassaemia minor and Cooley's disease or thalassaemia major Ann Eugen. , 16, 299.

21.

Danes, B.S. and Bearn, A.G. (1968). Genetic cell marker in cystic fibrosis of pancreas Lancet , 1, 1061.

22.

Steele, M.V. and Breg, W.R. (1966). Chromosomal analysis of Human Amniotic-Fluid cells Lancet , 1, 383.

23.

Fujimoto, W.Y. , Seegmiller, J.E. , Uhlendorf , B.W. and Jacobson , C.B. (1968). Biochemical diagnosis of an X-linked disease in utero Lancet, 2, 511.

24.

Clarke, C.A. , Finn, R. , Lehane , D. , Mcconnell, R.B. , Sheppard, P.M. and Woodrow, J.C.

Dose of anti-D gamma globulin in prevention of Rh-haemolytic disease of the newborn

Brit. med. J. , 1, 213.

25.

Schull, W.J. (1958). Empirical Risks in Consanguineous Marriages: Sex Ratio, Malformation and Viability Amer. J. Hum. Genet., 10, 294.

26.

Slatis, H.M. , Reis, R.H. and Hoene, R.E. (1958). Consanguineous marriages in the Chicago region Amer. J. Hum. Genet. , 10, 446.

27.

Stevenson, A.C. , Johnston, H.A. , Stewart , M.I.P. and Goldring , D.R. (1966). Congenital Malformations. A Report of a Study of series of Consecutive Births in 24 Centres Bull W.H.O. Suppl. 34.