Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome. (2021)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41436-021-01246-2
PubMed Identifier: 34345025
Publication URI: http://europepmc.org/abstract/MED/34345025
Type: Journal Article/Review
Volume: 23
Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics
Issue: 11
ISSN: 1098-3600