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Dentinogenesis imperfecta type II in Swedish children and adolescents

BACKGROUND: Dentinogenesis imperfecta (DGI) is a heritable disorder of dentin. Genetic analyses have found two subgroups in this disorder: DGI type I, a syndromic form associated with osteogenesis imperfecta (OI), and DGI type II, a non-syndromic form. The differential diagnosis between types I and...

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Detalles Bibliográficos
Autores principales:	Andersson, K., Malmgren, B., Åström, E., Dahllöf, G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106925/ https://www.ncbi.nlm.nih.gov/pubmed/30134932 http://dx.doi.org/10.1186/s13023-018-0887-2

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