Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference18 articles.
1. Distal 12p deletion in a stillborn infant
2. Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome
3. Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
4. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
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