22q13 deletion syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference32 articles.
1. Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients.
2. The DNA sequence of human chromosome 22
3. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
4. 1990. Chromosome 22, ring 22. In: editor. Birth defects encyclopedia, volume 1. Dover, MA: Center for Birth Defects Information Services. p 394.
5. Phenotypic variation in two patients with a ring chromosome 22
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