Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population. (2022)

First Author: Kingdom R

Attributed to: UK Biobank (core renewal) funded by MRC

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