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Dentinogenesis Imperfecta

Known as: Dentinogenesis Imperfecta [Disease/Finding], Imperfecta, Dentinogenesis 
An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops… 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
AIM The aim of this study was to assess the correlation between osteogenesis imperfecta (OI) and dentinogenesis imperfecta (DI… 
Review
2008
Review
2008
The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal… 
Review
2007
Review
2007
Osteogenesis imperfecta (OI) is the most common of the inherited connective tissue disorders that primarily affect bone. However… 
Highly Cited
2005
Highly Cited
2005
The mouse mutation fragilitas ossium (fro) leads to a syndrome of severe osteogenesis and dentinogenesis imperfecta with no… 
Highly Cited
2003
Highly Cited
2003
Dentin sialophosphoprotein (Dspp) is mainly expressed in teeth by the odontoblasts and preameloblasts. The Dspp mRNA is… 
Highly Cited
2001
Highly Cited
2001
We identified a nonsense mutation (Gln45stop) in exon 3 of the dentin sialophosphoprotein (DSPP) gene in a Chinese family with… 
Highly Cited
2000
Highly Cited
2000
Osteogenesis imperfecta (OI) is commonly subdivided into four clinical types. Among these, OI type IV clearly represents a… 
Highly Cited
1999
Highly Cited
1999
Review
1988
Review
1988
  • C. Witkop
  • Journal of oral pathology
  • 1988
  • Corpus ID: 40468091
The classification and prevalence of amelogenesis imperfecta is updated based upon new information in the literature. Problems…