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High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome.

Authors
Type
Published Article
Journal
Human Mutation
1098-1004
Publisher
Wiley Blackwell (John Wiley & Sons)
Publication Date
Volume
32
Issue
1
Pages
91–97
Identifiers
DOI: 10.1002/humu.21395
PMID: 21120947
Source
Medline

Abstract

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