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Article

Craniofacial anomalies in a murine model of heterozygous fibroblast growth factor 10 gene mutation.

Orthodontics & craniofacial research - 1 Feb 2024

Tan Jenny, Jones Matthew L M, Teague Warwick J, Ranjitkar Sarbin, Anderson Peter J

Abstract excerpt

OBJECTIVE: Dysregulation of Fibroblast Growth Factor 10 (FGF10), a member of the family of Fibroblast Growth Factor (FGF) proteins, has been implicated in craniofacial and dental anomalies, including craniosynostosis, cleft palate, and Lacrimo-Auriculo-Dento-Digital Syndrome. The aim of this murine study was to assess the craniofacial and dental phenotypes associated with a heterozygous FGF10 gene (FGF10+/- )...

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Identifiers

PMID: 37452556
DOI: 10.1111/ocr.12689

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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