Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance. (2023)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2023.100883
PubMed Identifier: 37154149
Publication URI: http://europepmc.org/abstract/MED/37154149
Type: Journal Article/Review
Volume: 25
Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics
Issue: 9
ISSN: 1098-3600