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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Bibliographische Detailangaben
Hauptverfasser: Lin, Wei-De, Lin, Shuan-Pei, Wang, Chung-Hsing, Tsai, Yushin, Chen, Chih-Ping, Tsai, Fuu-Jen
Format: Artigo
Sprache:Inglês
Veröffentlicht: Sociedade Brasileira de Genética 2011
Schlagworte:
Short Communication
Online Zugang: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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