Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia-Reference-Cited by-同舟云学术

Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia

Published:2017-01-24 Issue:3 Volume:23 Page:360-366
ISSN:1354-523X
Container-title:Oral Diseases
language:en
Short-container-title:Oral Dis

Author:

Li F¹,Liu Y¹,Liu H¹,Yang J¹,Zhang F²,Feng H¹

Affiliation:

1. Department of Prosthodontics; National Engineering Laboratory for Digital and Material Technology of Stomatology; Beijing Key Laboratory of Digital Stomatology; Peking University School and Hospital of Stomatology; Beijing China

2. Department of Pediatrics; Peking University School and Hospital of Stomatology; Beijing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/odi.12621/fullpdf

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4. A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family;Bai;BMC Med Genet,2010

5. Hypodontia: etiology, clinical features, and management;Dhanrajani;Quintessence Int,2002

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