Review of Recurrently Mutated Genes in Craniosynostosis Supports Expansion of Diagnostic Gene Panels. (2023)
Attributed to:
Congenital Anomalies - Patient-led Functional Genomics
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.3390/genes14030615
PubMed Identifier: 36980886
Publication URI: http://europepmc.org/abstract/MED/36980886
Type: Journal Article/Review
Volume: 14
Parent Publication: Genes
Issue: 3
ISSN: 2073-4425