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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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Detalles Bibliográficos
Autores principales: Ceyhan, Derya, Kirzioglu, Zuhal, Calapoglu, Nilufer Sahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260382/
https://www.ncbi.nlm.nih.gov/pubmed/25565750
http://dx.doi.org/10.4103/0975-962X.144717