RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia

Cleidocranial dysplasia (CCD) is an autosomal dominant human skeletal disorder comprising hypoplastic clavicles, wide cranial sutures, supernumerary teeth, short stature, and other skeletal abnormalities. It is known that mutations in the human RUNX2 gene mapped at 6p21 are responsible for CCD. We a...

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Main Authors: Lin, Wei-De, Lin, Shuan-Pei, Wang, Chung-Hsing, Tsai, Yushin, Chen, Chih-Ping, Tsai, Fuu-Jen
格式: Artigo
語言:Inglês
出版: Sociedade Brasileira de Genética 2011
主題:
Short Communication
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3115309/
https://ncbi.nlm.nih.gov/pubmed/21734816
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1415-47572011005000002
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