A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele. (2023)

First Author: Crane-Smith Z
Attributed to:  Congenital Anomalies: Patient-led Functional Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddad094

PubMed Identifier: 37364051

Publication URI: http://europepmc.org/abstract/MED/37364051

Type: Journal Article/Review

Volume: 32

Parent Publication: Human molecular genetics

Issue: 17

ISSN: 0964-6906