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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… 
Highly Cited
2010
Highly Cited
2010
Micro-flow imaging (MFI) has been shown to be more sensitive than light obscuration (LO) methods for measuring subvisible… 
Review
2008
Review
2008
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal… 
Highly Cited
2001
Highly Cited
2001
Dentinogenesis imperfecta 1 (DGI1, MIM 125490) is an autosomal dominant dental disease characterized by abnormal dentin… 
Review
2000
Review
2000
Abstract This paper presents a short review of three groups of tools which can be or are used for the tissue engineering of… 
Highly Cited
1995
Highly Cited
1995
Dentinogenesis imperfecta type II (DGI1) is an autosomal dominant disorder of dentin formation, which has been mapped to human… 
1971
1971
  • R. Jorgenson
  • Birth defects original article series
  • 1971
  • Corpus ID: 423287
Researchers have described three types of dentinogenesis imperfecta with similar dental abnormalities. Type I occurs in people…