Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank. (2020)
Attributed to:
UK Biobank (core renewal)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-020-0626-8
PubMed Identifier: 32327713
Publication URI: http://europepmc.org/abstract/MED/32327713
Type: Journal Article/Review
Volume: 28
Parent Publication: European journal of human genetics : EJHG
Issue: 9
ISSN: 1018-4813