Medical genetics

Berg, K., Fletcher, J. C., and Tranoy, K. E., Ethical guidelines for genetic screening and prenatal diagnosis: a proposal Personal communication, 1984.Google Scholar

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Davies, K. D., Jackson, J., Williamson, R., Harper, P. S., Ball, S., Sarfarazi, M., Meredith, L., and Frey, G., Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe. J. med. Genet.20 (1983) 259–263.Google Scholar

Fletcher, J. C., Ethics and trends in applied human genetics. Birth Defects: Original Article Series, Vol. 19 (5), pp. 143–158. March of Dimes Birth Defects Foundation (1983).Google Scholar

Galjaard, H., Genetic Metabolic Diseases. Early Diagnosis and Prenatal Analysis. Elsevier/North-Holland Biomedical Press, Amsterdam, New York, Oxford 1980.Google Scholar

Gusella, J. F., Wexler, N. W., Couneally, P. M., Naylor, S. C., Anderson, M. A., Tanzi, R. E., Watkins, A. C., Ottina, K., Wallace, M. R., Sakaguchi, A. Y., Young, A. B., Shoulson, J., Bonilla, E., and Martin, J. B., A polymorphic DNA marker genetically linked to Huntington's disease. Nature306 (1983) 234–238.Google Scholar

Humphries, S. E., and Williamson, R., Applicaiton of recombinant DNA technology to prenatal defection of inherited defects. Br. med. Bull.39 (1983) 343–347.Google Scholar

McKusick, V. A., Mendelian Inheritance in Man. Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes, 6th edn. The John Hopkins University Press, 1983.Google Scholar

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Medizinische Genetik. Informationsblatt der Schweiz. Ges. f. Med. Genetik No. 12 (1984).Google Scholar

Panny, S. R., Scott, A. F., Smith, K. D., Philips III, J. A., Kazazain, H. H., Talbot, C. C., and Boehm, C. D., Population heterogeneity of the Hpal restriction site associated with the β-globin gene: Implications for prenatal diagnosis. Am. J. hum. Genet.33 (1981) 25–35.Google Scholar

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Savoldelli, G., Schmid, W., and Schinzel, A., Prenatal diagnosis of cleft lip and palate by ultrasound. Prenatal Diag.2 (1982) 313–317.Google Scholar

Schinzel, A., Savoldelli, G., Briner, J., and Schubiger, G., Prenatal ultrasonographic diagnosis of Jeune syndrome (asphyxiating thoracic dysplasia), 1986, in press.Google Scholar

Schmid, W., Der Stand der pränatalen genetischen Diagnostik. Schweiz. Rundsch. f. med. Praxis8 (1984) 239–243.Google Scholar

Simoni, G., and Rossella, F., First trimester fetal karyotyping using chorionic villi: technical development and diagnostic application. Experientia42 (1986) 1097–1101.Google Scholar