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Genome-wide analysis identifies a role for common copy number variants in specific language impairment. (2015)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2014.296

PubMed Identifier: 25585696

Publication URI: http://europepmc.org/abstract/MED/25585696

Type: Journal Article/Review

Volume: 23

Parent Publication: European journal of human genetics : EJHG

Issue: 10

ISSN: 1018-4813