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1 tooth disorders such as dentin dysplasia and dentinogenesis imperfecta.
2 oring the Col1a2(oim) mutation (oim) express dentinogenesis imperfecta.
3                                              Dentinogenesis imperfecta (DGI) and dentin dysplasia (DD
4                                              Dentinogenesis imperfecta (DGI) and dentin dysplasia (DD
5                                              Dentinogenesis imperfecta (DGI) is characterized by disc
6           DSPP mutations in humans may cause dentinogenesis imperfecta (DGI), an autosomal dominant d
7 lt in human hereditary dental disorders like dentinogenesis imperfecta II (MIM 125420) and dentin dys
8 otein (dspp), a candidate gene implicated in dentinogenesis imperfecta II (MIM 125420), is significan
9 ations in this gene were identified in human dentinogenesis imperfecta II (Online Mendelian Inheritan
10  that develop tooth defects similar to human dentinogenesis imperfecta III with enlarged pulp chamber
11 nd shares some features of the human disease dentinogenesis imperfecta III.
12 p9-/- teeth displayed a phenotype similar to dentinogenesis imperfecta, including decreased dentin mi
13 s that may be accompanied by bone deformity, dentinogenesis imperfecta, short stature, and shortened
14 ns of a consanguineous family display severe dentinogenesis imperfecta, short stature, various skelet
15                                              Dentinogenesis Imperfecta type II (DGI-II) is a localize
16 ed to determine if DGI-III co-localized with dentinogenesis imperfecta type II (DGI-II), which has be
17 attering (SAXS) were performed on normal and dentinogenesis imperfecta type II (DI-II) teeth.
18 d Dmp2 genes at a position equivalent to the dentinogenesis imperfecta type II location on human 4q21
19            As recent studies have shown that dentinogenesis imperfecta type II results from mutation
20 tween, and shared chromosomal location with, dentinogenesis imperfecta type II, a second disorder of
21 trong candidate gene for the genetic disease dentinogenesis imperfecta type II.
22                                              Dentinogenesis imperfecta type III (DGI-III) is an autos
23 s classified as dentin dysplasia type II and dentinogenesis imperfecta types II and III.