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

Jenny TanMatthew L M JonesWarwick J TeagueSarbin RanjitkarPeter J Anderson

Published in: Orthodontics & craniofacial research (2023)

mutation was associated with craniomaxillary skeletal hypoplasia that probably arose from deficient (delayed) intramembranous ossification of the sutured bones. Overall, the skeletal and dental data suggest that the FGF10 gene plays an important role in the aetiology of craniofacial dysmorphology and malocclusion.

Keyphrases

electronic health record
early onset
copy number
genome wide
oral health
big data
dna methylation
deep learning