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Article

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

Archives italiennes de biologie - 1 Sept 2011

Locuratolo Nicoletta, Baffico M, Baldi M, Parisi V, Micacchi F, Angelucci V, Rojas Beccaglia M, Pirro C, Fattapposta Francesco

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Receptor, Fibroblast Growth Factor, Type 2

Source

Identifiers

PMID: 22028092
DOI: 10.4449/aib.v149i3.1379

Genes

FGFR2

Provenance

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Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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A novel fibroblast growth factor receptor 2 (FGFR2) mutation associated with a mild Crouzon syndrome.PMID 22028092Read ↗

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Effect on splicing of a silent FGFR2 mutation in Crouzon syndromeSemantic proximity Read ↗

Bilateral exophthalmos: Report of a case and review of a fibroblast growth factor receptor 2 mutation associated with non-penetrant Crouzon syndrome.Semantic proximity Read ↗

A novel FGFR2 mutation in tyrosine kinase II domain, L617F, in Crouzon syndrome.Semantic proximity Read ↗

FGFR2 splice site mutations in Crouzon and Pfeiffer syndromes: two novel variants.Semantic proximity Read ↗

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.Semantic proximity Read ↗

The Fgfr2 W290R mouse model of Crouzon syndrome.Semantic proximity Read ↗

A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.Semantic proximity Read ↗

Surgical Result and Identification of FGFR2 Variants Using Whole-Exome Sequencing in a Chinese Family With Crouzon Syndrome.Semantic proximity Read ↗

Current Understanding of Crouzon Syndrome Pathophysiology and New Therapeutic Approaches.Semantic proximity Read ↗

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