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Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank. (2020)

First Author: Williams SG

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