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