Validation of a genome-wide association study implied that SHTIN1 may involve in the pathogenesis of NSCL/P in Chinese population

Orofacial clefts are among the most common birth defects in humans worldwide. A large-scale, genome-wide association study (GWAS) in the Chinese population recently identified several genetic risk variants for nonsyndromic cleft lip with or without cleft palate (NSCL/P). We selected 16 significant S...

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Detalles Bibliográficos
Autores principales: Wang, Yirui, Sun, Yimin, Huang, Yongqing, Pan, Yongchu, Yin, Aihua, Shi, Bing, Du, Xuefei, Ma, Lan, Lan, Feifei, Jiang, Min, Shi, Jiayu, Zhang, Lei, Xiao, Xue, Zhou, Zhongwei, Jiang, Hongbing, Wang, Lin, Yang, Yinxue, Cheng, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5180092/
https://www.ncbi.nlm.nih.gov/pubmed/28008912
http://dx.doi.org/10.1038/srep38872

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