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Article

Craniosynostosis and related limb anomalies.

Novartis Foundation symposium - 1 Jan 2001

Wilkie A O, Oldridge M, Tang Z, Maxson R E

Abstract excerpt

Many genetically determined craniosynostosis syndromes feature limb anomalies, implying that pathways of cranial suture and limb morphogenesis share some identical components. Identification of heterozygous mutations in FGFR1, FGFR2, FGFR3, TWIST and MSX2 in craniosynostosis has focused particula...

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Source

Identifiers

PMID: 11277076
DOI: 10.1002/0470846658.ch9

Genes

FGFR2
MSX2
FGFR1
FGFR3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-11277076-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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