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Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies

AIM: To search for mutations on the MSX1 gene and to present a genetic basis for non-syndromic tooth agenesis in conjunction with dental anomalies in a Turkish population. MATERIALS AND METHODS: The patients included in this study were otherwise healthy, with ages ranging from seven to eighteen year...

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Detalhes bibliográficos
Publicado no:Indian J Dent
Main Authors: Ceyhan, Derya, Kirzioglu, Zuhal, Calapoglu, Nilufer Sahin
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4260382/
https://ncbi.nlm.nih.gov/pubmed/25565750
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0975-962X.144717
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