Association of AXIN2 gene polymorphisms with nonsyndromic oligodontia in Turkish families
Tooth agenesis is the most common developmental abnormality of the human dentition characterized by the congenital absence of one or more permanent teeth. Oligodontia is the term used to describe severe tooth agenesis, where six or more permanent teeth are missing. The WNT gene pathway regulates mul...
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| Main Authors: | , , , |
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| Format: | Book |
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University Library System, University of Pittsburgh,
2016-10-01T00:00:00Z.
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A1234.567 |
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