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Article

FGFR2 gene mutation (Tyr375Cys) in a new case of Beare-Stevenson syndrome.

American journal of medical genetics - 1 Apr 1998

Krepelová A, Baxová A, Calda P, Plavka R, Kapras J

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Source

Identifiers

PMID: 9545103

Genes

FGFR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Research trail→

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FGFR2 gene mutation (Tyr375Cys) in a new case of Beare-Stevenson syndrome.PMID 9545103Read ↗

The first Korean case of Beare-Stevenson syndrome with a Tyr375Cys mutation in the fibroblast growth factor receptor 2 gene.Semantic proximity Read ↗

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A novel fibroblast growth factor receptor 2 (FGFR2) mutation associated with a mild Crouzon syndrome.Semantic proximity Read ↗

Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.Semantic proximity Read ↗

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Cardio-facio-cutaneous syndrome with BRAF gene mutation: A case report and literature review.Semantic proximity Read ↗

A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome.Semantic proximity Read ↗

A case of Beare-Stevenson syndrome with a broad spectrum of features and a review of the FGFR2 Y375C mutation phenotype.Semantic proximity Read ↗

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