Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. (2020)
Attributed to:
MRC Centre for Neurodevelopmental Disorders
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