Add to ORKGDentinogenesis imperfecta (DI) is a genetic disorder characterized by dentin discoloration, tooth development irregularities, and decreased tooth strength. This autosomal dominant disorder is identified in individuals of all ages. There are three classifications of dentinogenesis imperfecta, each with varying presentations and causes. This report covers normal tooth development (odontogenesis), DI development, DI classifications, and the genes involved in this genetic disorder
In dental practice may be encountered a wide variability in the clinical dental phenotype of tooth n...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormali...
Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalit...
BackgroundDentinogenesis imperfecta (DI) is a rare debilitating hereditary disorder affecting dentin...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), compri...
The dentin sialophosphoprotein (DSPP) gene (4q21.3) encodes two major noncollagenous dentin matrix p...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Objective: Hereditary dentin defects can be grouped into three types of dentinogenesis imperfecta (D...
Dentinogenesis imperfecta (DGI) is an autosomal dominant disorder in which both the primary and the ...
The last research of calcified tissue like bones and teeth has provided new information with regard ...
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the developmen...
In dental practice may be encountered a wide variability in the clinical dental phenotype of tooth n...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormali...
Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalit...
BackgroundDentinogenesis imperfecta (DI) is a rare debilitating hereditary disorder affecting dentin...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), compri...
The dentin sialophosphoprotein (DSPP) gene (4q21.3) encodes two major noncollagenous dentin matrix p...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Objective: Hereditary dentin defects can be grouped into three types of dentinogenesis imperfecta (D...
Dentinogenesis imperfecta (DGI) is an autosomal dominant disorder in which both the primary and the ...
The last research of calcified tissue like bones and teeth has provided new information with regard ...
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the developmen...
In dental practice may be encountered a wide variability in the clinical dental phenotype of tooth n...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...