Dentinogenesis imperfecta without osteogenesis imperfecta
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Genetic data have revealed that the absence of Bacillus subtilis RecO and one of the end-processing avenues (AddAB or RecJ… Expand Micro-flow imaging (MFI) has been shown to be more sensitive than light obscuration (LO) methods for measuring subvisible… Expand Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal… Expand Abstract A critical review of the different methods used nowadays for calculating tunneling currents and STM-images is presented… Expand Dentinogenesis imperfecta 1 (DGI1, MIM 125490) is an autosomal dominant dental disease characterized by abnormal dentin… Expand This study explores the use of water sorption/retention measures as alternative methodologies to the official methylene blue… Expand Abstract This paper presents a short review of three groups of tools which can be or are used for the tissue engineering of… Expand Dentinogenesis imperfecta type II (DGI1) is an autosomal dominant disorder of dentin formation, which has been mapped to human… Expand Two children of Austrian Ashkenazic Jewish background, related as second cousins, have a variant of opalescent dentin in their… Expand Researchers have described three types of dentinogenesis imperfecta with similar dental abnormalities. Type I occurs in people… Expand