Prognostic value of legumain in uveal melanoma

by WU, TONG, SUN, LEI, WU, YING, XIANG, RONG, LI, YUWEI, RONG, WEINING, SUN, FENGYUAN, WANG, NINGLI
Published 2016

Novel and Recurrent MYO7A Mutations in Usher Syndrome Type 1 and Type 2

by Rong, Weining, Chen, Xue, Zhao, Kanxing, Liu, Yani, Liu, Xiaoxing, Ha, Shaoping, Liu, Wenzhou, Kang, Xiaoli, Sheng, Xunlun, Zhao, Chen
Published 2014

Association of insulin-like growth factor-1 polymorphisms with high myopia in the Chinese population

by Zhuang, Wenjuan, Yang, Peizeng, Li, Zili, Sheng, Xunlun, Zhao, Jingjing, Li, Shanshan, Yang, Xueqiu, Xiang, Wei, Rong, Weining, Liu, Yani, Zhang, Fangxia
Published 2012

Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia

by Sheng, Xunlun, Chen, Xue, Lei, Bo, Chen, Rui, Wang, Hui, Zhang, Fangxia, Rong, Weining, Ha, Ruoshui, Liu, Yani, Zhao, Feng, Yang, Peizeng, Zhao, Chen
Published 2015

Targeted Next-Generation Sequencing Reveals Novel USH2A Mutations Associated with Diverse Disease Phenotypes: Implications for Clinical and Molecular Diagnosis

by Chen, Xue, Sheng, Xunlun, Liu, Xiaoxing, Li, Huiping, Liu, Yani, Rong, Weining, Ha, Shaoping, Liu, Wenzhou, Kang, Xiaoli, Zhao, Kanxing, Zhao, Chen
Published 2014

Targeted Next-generation Sequencing Reveals Novel EYS Mutations in Chinese Families with Autosomal Recessive Retinitis Pigmentosa

by Chen, Xue, Liu, Xiaoxing, Sheng, Xunlun, Gao, Xiang, Zhang, Xiumei, Li, Zili, Li, Huiping, Liu, Yani, Rong, Weining, Zhao, Kanxing, Zhao, Chen
Published 2015

CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability

by Minegishi, Yuriko, Sheng, XunLun, Yoshitake, Kazutoshi, Sergeev, Yuri, Iejima, Daisuke, Shibagaki, Yoshio, Monma, Norikazu, Ikeo, Kazuho, Furuno, Masaaki, Zhuang, Wenjun, Liu, Yani, Rong, Weining, Hattori, Seisuke, Iwata, Takeshi
Published 2016