WNT10A and isolated hypodontia

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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書目詳細資料
Main Authors:	Kantaputra P., Sripathomsawat W.
格式:	雜誌
出版:	2017
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
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!
機構:	Chiang Mai University

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