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Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function. (2023)

First Author: Tooze RS

Attributed to: New molecular mechanisms of craniosynostosis funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmg-2022-108946

PubMed Identifier: 36543535

Publication URI: http://europepmc.org/abstract/MED/36543535

Type: Journal Article/Review

Volume: 60

Parent Publication: Journal of medical genetics

Issue: 7

ISSN: 0022-2593