Disease: Dentinogenesis imperfecta- shields type 3
- Brittle teeth with brittle bone in a family for four generations: Case report and literature review
- Dentin defects caused by a Dspp<sup>-1</sup> frameshift mutation are associated with the activation of autophagy
- Dentinogenesis imperfecta. Scanning electron microscopic study and microanalysis
- DSPP mutation in dentinogenesis imperfecta Shields type II
- Hereditary dentin defects
- Identification of a novel mutation of DSPP gene in a Chinese family affected with dentinogenesis imperfecta shields type II
- Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields type II patients
- Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification
- The Modified Shields Classification and 12 Families with Defined <em>DSPP</em> Mutations
- The Modified Shields Classification and 12 Families with Defined DSPP Mutations