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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1948-2017
0102019482016

Papers overview

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2006
2006
Dentinogenesis imperfecta (DGI) and dentin dysplasia (DD) are allelic disorders that primarily affect the formation of tooth… (More)
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2005
2005
The mouse mutation fragilitas ossium (fro) leads to a syndrome of severe osteogenesis and dentinogenesis imperfecta with no… (More)
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2004
2004
The dentin sialophosphoprotein (DSPP) gene (4q21.3) encodes two major noncollagenous dentin matrix proteins: dentin sialoprotein… (More)
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2004
2004
Dentinogenesis imperfecta (DI) type II, an inherited disorder affecting dentin, has been linked to mutations in the dentin… (More)
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2004
2004
The current system for the classification of hereditary defects of tooth dentin is based upon clinical and radiographic findings… (More)
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Highly Cited
2003
Highly Cited
2003
Dentin sialophosphoprotein (Dspp) is mainly expressed in teeth by the odontoblasts and preameloblasts. The Dspp mRNA is… (More)
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Highly Cited
2002
Highly Cited
2002
Osteogenesis imperfecta (OI) is a heritable disease of bone in which the hallmark is bone fragility. Usually, the disorder is… (More)
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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… (More)
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2001
2001
Dentinogenesis imperfecta (DI) type 2 is a disease inherited in a simple autosomal dominant mode. As soon as the teeth erupt the… (More)
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Highly Cited
2000
Highly Cited
2000
Osteogenesis imperfecta (OI) is commonly subdivided into four clinical types. Among these, OI type IV clearly represents a… (More)
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