Waardenburg syndrome type I: Dental phenotypes and genetic analysis of an extended family

BACKGROUND: The aim of this study was to describe the pattern of inheritance and the clinical features in a large family with Waardenburg syndrome type I (WS1), detailing the dental abnormalities and screening for PAX3 mutations. MATERIAL AND METHODS: To characterize the pattern of inheritance and c...

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Detalles Bibliográficos
Autores principales: Sólia-Nasser, Luciano, de Aquino, Sibele-Nascimento, Paranaíba, Lívia-Maris-R., Gomes, Andreia, dos-Santos-Neto, Pedro, Coletta, Ricardo-D., Cardoso, Aline-Francoise, Frota, Ana-Cláudia, Martelli-Júnior, Hercílio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867205/
https://www.ncbi.nlm.nih.gov/pubmed/27031059
http://dx.doi.org/10.4317/medoral.20789

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867205/
https://www.ncbi.nlm.nih.gov/pubmed/27031059
http://dx.doi.org/10.4317/medoral.20789

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