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Article

Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.

Journal of medical genetics - 1 Aug 2005

McGillivray G, Savarirayan R, Cox T C, Stojkoski C, McNeil R, Bankier A, Bateman J F, Roscioli T, Gardner R J M, Lamandé S R

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Topics

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Share to Abnormalities, Multiple
Share to Craniosynostoses
Share to Genetic Testing
Share to Intellectual Disability

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Protein Structure, Tertiary

Share to Receptor, Fibroblast Growth Factor, Type 2

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Source

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Identifiers

PMID: 16061565
DOI: 10.1136/jmg.2004.027888
PMCID: PMC1736114

Genes

FGFR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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