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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...
Autores principales: | Ceyhan, Derya, Kirzioglu, Zuhal, Calapoglu, Nilufer Sahin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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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 |
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