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- W2368984893 abstract "Objective: To investigate and analyze phenotypes in Chinese families with dentinogenesis imperfecta(DGI) and dentin dysplasia(DD).Methods: Chinese families with DGI and DD were collected with ascertainment.The hereditary modes were determined according to the investigation on the family pedigrees respectively.Based clinical manifestations and radiographic features,phenotype analysis was performed on affected individuals in each family.Results: A total of 4 Chinese families with DGI or DD were enrolled into the study.Dentinogenesis imperfecta type Ⅱ(DGI-Ⅱ) with autosomal dominant inheritance was determined in family Ⅰ,Ⅱ and Ⅲ.The proband in family Ⅳ was diagnosed as DGI-Ⅱ.Discrepancy or consistency among phenotypes existed in investigated families and individuals.Conclusion: Dentinogenesis imperfecta or dentin dysplasia in subtypes with an isolated trait in dentin has some common phenotypes.They could be considered as the same type of dentin defects when further studying the pathogenic mechanism." @default.
- W2368984893 created "2016-06-24" @default.
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- W2368984893 date "2006-01-01" @default.
- W2368984893 modified "2023-09-23" @default.
- W2368984893 title "Analysis on Phenotypes in Families with Dentinogenesis Imperfecta and Dentin Dysplasia." @default.
- W2368984893 hasPublicationYear "2006" @default.
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