📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

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