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Article

Fibroblast growth factor receptor 3 mutations in achondroplasia and related forms of dwarfism.

Reviews in endocrine & metabolic disorders - 1 Dec 2002

Horton William A, Lunstrum Gregory P

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

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Source

Identifiers

PMID: 12424440
DOI: 10.1023/a:1020914026829

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

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

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