Prenatal Diagnosis and Carrier Detection for a Point Mutation in UBE3A Causing Angelman Syndrome
- 1 November 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (5) , 1561-1563
- https://doi.org/10.1086/302120
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
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