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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. (2020)

First Author: Zhao Y
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/10.1016/j.ajhg.2019.11.010

PubMed Identifier: 31870554

Publication URI: http://europepmc.org/abstract/MED/31870554

Type: Journal Article/Review

Volume: 106

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297