Familial non-syndromic oligodontia
Oligodontia, a rare genetic disorder, represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and is usually the feature of a syndrome. Its occurrence as an isolated entity is even rarer. This article reports non-syndromic oligodontia in two siblings. One c...
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Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
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A1234.567 |
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