Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: A study of four individuals in two families
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference13 articles.
1. 18p- Syndrome resulting from 14q/18q ?dicentric? fusion translocation
2. Fetal loss and familial chromosome I translocations*
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