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Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. (2017)

First Author: Bassett AS

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/10.1176/appi.ajp.2017.16121417

PubMed Identifier: 28750581

Publication URI: http://europepmc.org/abstract/MED/28750581

Type: Journal Article/Review

Volume: 174

Parent Publication: The American journal of psychiatry

Issue: 11

ISSN: 0002-953X