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Brittle teeth with brittle bone in a family for four generations: Case report and literature review

Dentinogenesis imperfect (DI) is a hereditary dentine disorder affecting both deciduous and permanent teeth. DI is caused by mutations in genes encoding for type I collagen leading to discoloration of teeth. Shield around 30 years ago classified DI into 3 types (type I, II, and III). DI type I is as...

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Detalhes bibliográficos
Main Authors: Shilpa, P. S., David, Chaya M., Kaul, Rachna, Sanjay, C. J., Narayan, B. K. Ram
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3425106/
https://ncbi.nlm.nih.gov/pubmed/22919223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.96822
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