Molecular and phenotypic characterization of ring chromosome 22
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference64 articles.
1. FISH-mapping of a 100-kb terminal 22q13 deletion
2. Autism: Towards an Integration of Clinical, Genetic, Neuropsychological, and Neurobiological Perspectives
3. Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies
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