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Article

Fibroblast growth factor receptor 3 (FGFR3) gene G1138A mutation in Chinese patients with achondroplasia.

Human mutation - 1 Jan 1996

Wang T R, Wang W P, Hwu W L, Lee M L

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 8844216
DOI: 10.1002/(SICI)1098-1004(1996)8:2<178::AID-HUMU10>3.0.CO;2-#

Genes

FGFR3

Variants

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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Fibroblast growth factor receptor 3 (FGFR3) gene G1138A mutation in Chinese patients with achondroplasia.PMID 8844216Read ↗

FGFR3 gene mutations in transmembrane domain in Chinese achondroplasia and hypochondroplasia patients.Semantic proximity Read ↗

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Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene.Semantic proximity Read ↗

Molecular defects in achondroplasia and the effects of growth hormone treatment.Semantic proximity Read ↗

[Mutation analysis of fibroblast growth factor receptor 3 gene in an achondroplasia family].Semantic proximity Read ↗

Fibroblast growth factor receptor 3 mutations in achondroplasia and related forms of dwarfism.Semantic proximity Read ↗

[Mutations of the fibroblast growth factor receptor 3 gene in achondroplasia].Semantic proximity Read ↗

Identification and in silico characterization of p.G380R substitution in FGFR3, associated with achondroplasia in a non-consanguineous Pakistani family.Semantic proximity Read ↗

Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report.Semantic proximity Read ↗

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.Semantic proximity Read ↗

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