The genetics of non-syndromic dentinogenesis imperfecta: a systematic review. [PDF]
Gilani M, Saikia A, Anthonappa R.
europepmc +1 more source
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated patients with different types and forms of OI, (2) degree of dentin dysplasia in relation to type and form of OI and clinical, radiographic, and microscopic
Barbro Malmgren (4022861)
core
Effects of dentinogenesis imperfecta, sex, and tooth type on the compositional and structural organization of the dentin-enamel junction in the osteogenesis imperfecta murine model. [PDF]
Katebifar S +4 more
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X-ray microanalysis of dentine in primary teeth diagnosed Dentinogenesis Imperfecta type II. [PDF]
Sabel N +3 more
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A Novel Variant in Dentin Sialophosphoprotein (DSPP) Gene Causes Dentinogenesis Imperfecta Type III: Case Report. [PDF]
Wang Y, Xu X, Ding Y, Yuan G.
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Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling. [PDF]
Hassib NF +3 more
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A homozygous SP7/OSX mutation causes osteogenesis and dentinogenesis imperfecta with craniofacial anomalies. [PDF]
Al-Mutairi DA +5 more
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Management of Dentinogenesis Imperfecta: A Report of Two Cases. [PDF]
Kaur A, Kumar S, Karda B, Chibh R.
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A family study of dentinogenesis imperfecta shields type II caused by a novel DSPP mutation and investigations on the isolated stem cells from human exfoliated deciduous teeth. [PDF]
Gao Q +6 more
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Mutant Dentin Sialophosphoprotein Causes Dentinogenesis Imperfecta. [PDF]
Liang T +5 more
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