LEF-1 Regulates Tyrosinase Gene Transcription In Vitro

Por Wang, Xueping, Liu, Yalan, Chen, Hongsheng, Mei, Lingyun, He, Chufeng, Jiang, Lu, Niu, Zhijie, Sun, Jie, Luo, Hunjin, Li, Jiada, Feng, Yong
Publicado no PLoS One (2015)

A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing

Por Liu, Yalan, Wang, Lili, Feng, Yong, He, Chufeng, Liu, Deyuan, Cai, Xinzhang, Jiang, Lu, Chen, Hongsheng, Liu, Chang, Wu, Hong, Mei, Lingyun
Publicado no PLoS One (2016)

Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2

Por Sun, Jie, Hao, Ziqi, Luo, Hunjin, He, Chufeng, Mei, Lingyun, Liu, Yalan, Wang, Xueping, Niu, Zhijie, Chen, Hongsheng, Li, Jia-Da, Feng, Yong
Publicado no J Hum Genet (2017)

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

Por Wu, Hong, Feng, Yong, Jiang, Lu, Pan, Qian, Liu, Yalan, Liu, Chang, He, Chufeng, Chen, Hongsheng, Liu, Xueming, Hu, Chang, Hu, Yiqiao, Mei, Lingyun
Publicado no PLoS One (2016)

A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family

Por Niu, Zhijie, Feng, Yong, Mei, Lingyun, Sun, Jie, Wang, Xueping, Wang, Juncheng, Hu, Zhengmao, Dong, Yunpeng, Chen, Hongsheng, He, Chufeng, Liu, Yalan, Cai, Xinzhang, Liu, Xuezhong, Jiang, Lu
Publicado no PLoS One (2017)

Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family

Por Wang, Honghan, Wang, Xinwei, He, Chufeng, Li, Haibo, Qing, Jie, Grati, Mhamed, Hu, Zhengmao, Li, Jiada, Hu, Yiqiao, Xia, Kun, Mei, Lingyun, Wang, Xingwei, Yu, Jianjun, Chen, Hongsheng, Jiang, Lu, Liu, Yalan, Men, Meichao, Zhang, Hailin, Guan, Liping, Xiao, Jingjing, Zhang, Jianguo, Liu, Xuezhong, Feng, Yong
Publicado no J Hum Genet (2015)