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Dentinogenesis Imperfecta : A Family which was Affected for Over Three Generations
Dentinogenesis Imperfecta (DI) or hereditary opalescent dentin is inherited in a simple autosomal dominant mode with high penetrance and low mutation rates. It generally affects both the deciduous and the permanent dentitions. DI corresponds to a localized form of mesodermal dysplasia which is obser...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
JCDR Research and Publications (P) Limited
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3782979/ https://ncbi.nlm.nih.gov/pubmed/24086922 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2013/5723.3286 |
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