Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population. (2022)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2022.05.011
PubMed Identifier: 35700724
Publication URI: http://europepmc.org/abstract/MED/35700724
Type: Journal Article/Review
Volume: 109
Parent Publication: American journal of human genetics
Issue: 7
ISSN: 0002-9297