Antenatal diagnosis of genetic disease / edited by A.E.H. Emery.

Date:
1973
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Antenatal diagnosis of genetic disease / edited by A.E.H. Emery. Source: Wellcome Collection.

    172/192 (page 154)
    154 ANTENATAL DIAGNOSIS OF GENETIC DISEASE implications for relatives at risk. (Submitted.) Emery, A. E. H. & Morton, R. (1968). Genetic counselling in lethal X-linked disorders. Acta genetica {Basel) 18, 534—542. Emery, A. E. H., Nelson, M. M. & Mayo, O. (1971). Antenatal diagnosis and the muscular dystrophies. Proceedings of the Second International Congress of Neuropathology, pp. 13-18. Edited by G. Serratrice. Paris; Expansion scienti¬ fique. Emery, A. E. H. & Smith, C. (1970). Ascertainment and prevention of genetic disease. British Medical Journal iii, 636-637. Falconer, D. S. (1965). The inheritance of liability to certain diseases, estimated from the incidence among relatives. Annals of Human Genetics 29, 51-76. Fraser, G. R. (1972). The short-term reduction in birth incidence of recessive diseases as a result of genetic counselling after the birth of an affected child. Human Heredity 22, 1-6. Fraser, G. R. & Motulsky, A. G. (1968). Genetic effects of selective abortion for inherited disease. American Journal of Human Genetics 20, 489 (abstract). Friedman, T. (1972). Prenatal diagnosis of genetic disease. Scientific American 225, ЪАгЛ2. Hollenberg, M. D., Kabach, M. N. & Kazazian, H. H. (1971). Adult haemoglobin synthesis of reticulocytes for the human fetus at midtrimester. Science, New York 174, 698-702. King, J. L. (1965). The effect of litter culling—or family plannmg—on the rate of natural selection. Genetics 51, 425-429. McKeov/n, T. (1968). Screening in Medical Care. Oxford University Press. McKusick, V. A. (1968). Family-oriented follow-up. Journal of Chronic Disease 22, 1-7. Mayo, O. (1970). The use of linkage in genetic counselling. Human Heredity 20, 473-485. Milunsky, A., Littlefield, J. W., Kanfer, J. N., Kolodny, E. H., Shih, V. E. & Atkins, L. (1971). Prenatal genetic diagnosis. New England Journal of Medicine 283, 1498-1504. Morton, N. E., Stevenson, C. & Harris, D. E. (1972). Genetic counselling as an outcome of segregation analysis. (Submitted.) Motulsky, A. G., Fraser, G. R. & Felsenstein, J. (1971). Public health and long- term genetic implications of intrauterine diagnosis and selective abortion. Birth Defects 7, 22-36. Murphy, E. A. (1969). Considerations in genetic counselling. American Academy of General Practice 40, 102-110. Murphy, E. A. (1970). The ENSU scoring system in genetic counselling. Annals of Human Genetics 34, 73-78. Murphy, E. A. & Mutalik, G. S. (1969). The application of Bayesian methods in genetic counselling. Human Heredity 19, 126-151. Newcombe, H. B. (1967). Present and long-term objectives of the British Colum¬ bia Population Study. Proceedings of the Third Congress of Human Genetics. pp. 291-313. Baltimore: Johns Hopkins Press. Penrose, L. S. & Smith, G. F. (1966). Down's anomaly. London: Churchill. Roberts, D. F., Chavez, J. & Court, S. D. M. (1970). The genetic component in child mortality. Archives of Disease in Childhood 45, 33-38. Smith, C. (1970). Ascertaining those at risk in the prevention and treatment of genetic disease. In Modern Trends in Human Genetics, vol. 1, p. 350. Edited by A. E. H. Emery. London: Butterworth. Smith, C. (1971). Recurrence risks for multifactorial inheritance. American Journal of Human Genetics 23, 578-588.