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Famlial nonsyndromic oligodontia
Oligodontia is one of the most common developmental abnormalities in humans. The present case report highlights the features of oligodontia in a 12-year-old male patient which was managed successfully with multidisciplinary approach. Familial oligodontia represents as an absence of varying numbers o...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3514934/ https://ncbi.nlm.nih.gov/pubmed/23230360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.101088 |
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