Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. (2020)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41591-020-1103-1

PubMed Identifier: 33169016

Publication URI: http://europepmc.org/abstract/MED/33169016

Type: Journal Article/Review

Volume: 26

Parent Publication: Nature medicine

Issue: 12

ISSN: 1078-8956