Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia

Craniofacial microsomia (CFM) is a rare congenital anomaly that involves immature derivatives from the first and second pharyngeal arches. The genetic pathogenesis of CFM is still unclear. Here we interrogate 0.9 million genetic variants in 939 CFM cases and 2,012 controls from China. After genotypi...

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Detalles Bibliográficos
Autores principales: Zhang, Yong-Biao, Hu, Jintian, Zhang, Jiao, Zhou, Xu, Li, Xin, Gu, Chaohao, Liu, Tun, Xie, Yangchun, Liu, Jiqiang, Gu, Mingliang, Wang, Panpan, Wu, Tingting, Qian, Jin, Wang, Yue, Dong, Xiaoqun, Yu, Jun, Zhang, Qingguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748111/
https://www.ncbi.nlm.nih.gov/pubmed/26853712
http://dx.doi.org/10.1038/ncomms10605

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