Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. (2020)
Attributed to:
Intellectual Disability and Mental Health: Assessing Genomic Impact on Neurodevelopment (IMAGINE)
funded by
MRC
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