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Dentinogenesis imperfecta without osteogenesis imperfecta

Known as: DENTINOGENESIS IMPERFECTA 1, OPALESCENT DENTIN, DGI-II 
 
National Institutes of Health

Papers overview

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2015
2015
Genetic data have revealed that the absence of Bacillus subtilis RecO and one of the end-processing avenues (AddAB or RecJ… Expand
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2010
2010
Micro-flow imaging (MFI) has been shown to be more sensitive than light obscuration (LO) methods for measuring subvisible… Expand
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2003
2003
We present a theoretical analysis of low-temperature quenching of one-dimensional Frenkel excitons that are localized by moderate… Expand
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Highly Cited
2001
Highly Cited
2001
Dentinogenesis imperfecta 1 (DGI1, MIM 125490) is an autosomal dominant dental disease characterized by abnormal dentin… Expand
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2001
2001
In Portugal the EEC membership represented a major change in Portuguese Administration functioning. This article uses the new… Expand
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1995
1995
Dentinogenesis imperfecta type II (DGI1) is an autosomal dominant disorder of dentin formation, which has been mapped to human… Expand
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1985
1985
Two children of Austrian Ashkenazic Jewish background, related as second cousins, have a variant of opalescent dentin in their… Expand
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1981
1981
Several methods of treating dentinogenesis imperfecta have been reported as successful, but long-term followup is necessary to… Expand
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1971
1971
Researchers have described three types of dentinogenesis imperfecta with similar dental abnormalities. Type I occurs in people… Expand
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1954
1954
  • G P Ivancie
  • Oral surgery, oral medicine, and oral pathology
  • 1954
  • Corpus ID: 37521621
Researchers have described three types of dentinogenesis imperfecta with similar dental abnormalities. Type I occurs in people… Expand
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