Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration a european collaborative study on prenatal diagnoses 1981

Author:

Stene Jon,Stene Eeva,Mikkelsen Margareta

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference36 articles.

1. Dermatoglyphics in parents of children with trisomy 21

2. (1979). European collaborative study on structural chromosome anomalies in prenatal diagnosis. Group report. In: , (Eds). Prenatal Diagnosis: Proceedings of the 3rd European Conference on Pretiatol Diagnosis of Genetic Disorders. Stuttgart: Enke. 35–54.

3. RISK OF PARENTS WHO HAVE HAD ONE CHILD WITH DOWN'S SYNDROME (MONGOLISM) HAVING ANOTHER CHILD SIMILARLY AFFECTED

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