Genetic Aspects of Dentinogenesis Imperfecta
Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormalities in the dentin of the developing teeth and occurring at a rate of about 1 in 8000 births. The expression of DI shows a high penetrance and a low mutation rate. Two main types of DI appear to exist...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Faculty of Dentistry, Universitas Indonesia,
2015-10-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |