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