📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

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