Dentin dysplasia type I—novel findings in deciduous and permanent teeth

BACKGROUND: Dentin dysplasia type I (DD-I) is a rare autosomal dominant hereditary disorder which seriously affects the root development of teeth, causing spontaneous tooth loss (in teenagers). At present, the study of DD-I focuses on familial and phenotypic analyses and reports regarding the ultras...

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Detalles Bibliográficos
Autores principales: Ye, Xin, Li, Kunyang, Liu, Ling, Yu, Fangfang, Xiong, Fu, Fan, Yun, Xu, Xiangmin, Zuo, Chunran, Chen, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689058/
https://www.ncbi.nlm.nih.gov/pubmed/26693824
http://dx.doi.org/10.1186/s12903-015-0149-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689058/
https://www.ncbi.nlm.nih.gov/pubmed/26693824
http://dx.doi.org/10.1186/s12903-015-0149-9

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