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Am J Med Genet. 1993 Apr 1;46(1):2-6.

Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.

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1
Genetics Division, Children's Hospital, Boston, Massachusetts.

Abstract

The majority of patients with Angelman syndrome and Prader-Willi syndrome have a cytogenetic and molecular deletion of chromosome 15q11q13 with the primary difference being in the parental origin of deletion. Our current understanding of the cytogenetics and molecular genetics of these 2 clinically distinct syndromes will be discussed in this review.

PMID:
8388170
DOI:
10.1002/ajmg.1320460103
[Indexed for MEDLINE]
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