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Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics. (2021)

First Author: Forsyth JK
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/cercor/bhab008

PubMed Identifier: 33638978

Publication URI: http://europepmc.org/abstract/MED/33638978

Type: Journal Article/Review

Volume: 31

Parent Publication: Cerebral cortex (New York, N.Y. : 1991)

Issue: 7

ISSN: 1047-3211