Section 2: Chromosome disease

Author:

Hamerton J. L.,Boué A.,Cohen M. M.,De La Chapelle A.,Hsu L. Y.,Lindsten J.,Mikkelsen M.,Robinson A.,Stengel-Rutkowski D.,Webb T.,Willey A.,Worton R.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference24 articles.

1. , and , 1978, The NICHD Amniocentesis Registry, The Safety and Accuracy of Mid-Trimester Amniocentesis. Washington, D.C. Department of Health, Education and Welfare. NIH Publication 78–190.

2. Medical Research Council, 1977, Diagnosis of genetic disease by amniocentesis during the second trimester of pregnancy: A Canadian study. Ottawa, Minister of Supply and Services Canada.

3. 1979, Maternal age specific incidence of chromosome aberrations at amniocentesis. In: , (Eds) Prenatal Diagnosis: Proceedings of the 3rd European Conference on Prenatal Diagnosis of Genetic Disorders. Stuttgart: Enke, 1–22.

4. 1979, Data from the inter-regional cytogenetic registry. Portland, Oregon. (Supported in part by contract no. HD-3-2713 from the National Institutes of Health, personal communication).

5. Series XIV;Hook,1978

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