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

Internet

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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