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