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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| Päätekijät: | , , , , |
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| Aineistotyyppi: | Kirja |
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Wolters Kluwer Medknow Publications,
2012-01-01T00:00:00Z.
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| Hyllypaikka: |
A1234.567 |
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| Nide 1 | Saatavissa |