Neurological aspects of del(1q) syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference30 articles.
1. Terminal deletion of (1)(q42) and its phenotypical manifestations
2. Report of the committee on the genetic constitution of chromosome 1
3. Terminal long-arm deletion of chromosome 1 in a male infant
4. Terminal deletion of chromosome 1(q43) in a female infant.
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