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Article

Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.

The Ulster medical journal - 1 May 2001

Hughes J, Nevin N C, Morrison P J

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Share to Abnormalities, Multiple
Share to Chromosomes, Human, Pair 4
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Protein-Tyrosine Kinases

Share to Receptor, Fibroblast Growth Factor, Type 3

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Identifiers

PMID: 11428324
PMCID: PMC2449219

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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