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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. (2014)

First Author: Rees E

Attributed to: MRC Centre for Neuropsychiatric Genetics and Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddt540

PubMed Identifier: 24163246

Publication URI: http://europepmc.org/abstract/MED/24163246

Type: Journal Article/Review

Volume: 23

Parent Publication: Human molecular genetics

Issue: 6

ISSN: 0964-6906