WNT10A and isolated hypodontia
WNT10A has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive SchÖpf-Schulz-Passarge syndrome to odonto-onycho-dermal dysplasia and autosomal dominant hypodontia. We report WNT10A mutations in an American family of which four members are affected with is...
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| Main Authors: | , |
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| 格式: | 雜誌 |
| 出版: |
2017
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| 在線閱讀: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955003002&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/43061 |
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| 機構: | Chiang Mai University |