References
Berg, K., Fletcher, J. C., and Tranoy, K. E., Ethical guidelines for genetic screening and prenatal diagnosis: a proposal Personal communication, 1984.
Cooper, D. N., and Schmidtke, J., DNA restriction fragment length polymorphisms and heterozygosity in the human genome. Hum. Genet.66 (1984) 1–16.
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.
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).
Galjaard, H., Genetic Metabolic Diseases. Early Diagnosis and Prenatal Analysis. Elsevier/North-Holland Biomedical Press, Amsterdam, New York, Oxford 1980.
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.
Humphries, S. E., and Williamson, R., Applicaiton of recombinant DNA technology to prenatal defection of inherited defects. Br. med. Bull.39 (1983) 343–347.
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.
Medizinische Genetik. Informationsblatt der Schweiz. Ges. f. Med. Genetik No. 6 (1981).
Medizinische Genetik. Informationsblatt der Schweiz. Ges. f. Med. Genetik No. 12 (1984).
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.
Schinzel, A., Savoldelli, G., Briner, J., Sigg, P., and Massini, C., Antley-Bixler syndrome in sisters: A term newborn and prenatally diagnosed fetus. Am. J. med. Genet.14 (1983) 139–147.
Savoldelli, G., Schmid, W., and Schinzel, A., Prenatal diagnosis of cleft lip and palate by ultrasound. Prenatal Diag.2 (1982) 313–317.
Schinzel, A., Savoldelli, G., Briner, J., and Schubiger, G., Prenatal ultrasonographic diagnosis of Jeune syndrome (asphyxiating thoracic dysplasia), 1986, in press.
Schmid, W., Der Stand der pränatalen genetischen Diagnostik. Schweiz. Rundsch. f. med. Praxis8 (1984) 239–243.
Simoni, G., and Rossella, F., First trimester fetal karyotyping using chorionic villi: technical development and diagnostic application. Experientia42 (1986) 1097–1101.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Schmid, W. Medical genetics. Experientia 42, 1086–1089 (1986). https://doi.org/10.1007/BF01941281
Issue Date:
DOI: https://doi.org/10.1007/BF01941281