Showing results (31-40 of 167) with videos related to
Sort By:
Pageof 17
Current Eye Research|December 22, 2009
Mutations in RPGR and RP2 of Chinese patients with X-linked retinitis pigmentosaYanli Ji, Juan Wang, Xueshan Xiao, et al.Molecular Vision|December 24, 2011
A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese familyXueshan Xiao, Xiangming Guo, Xiaoyun Jia, et al.Journal of Human Genetics|May 4, 2006
CSNB1 in Chinese families associated with novel mutations in NYXXueshan Xiao, Xiaoyun Jia, Xiangming Guo, et al.Current Eye Research|October 26, 2020
Variants in <i>RCBTB1</i> are Associated with Autosomal Recessive Retinitis Pigmentosa but Not Autosomal Dominant FEVRJunxing Yang, Xueshan Xiao, Wenmin Sun, et al.Molecular Medicine Reports|October 26, 2016
RGR variants in different forms of retinal diseases: The undetermined role of truncation mutationsJiali Li, Xueshan Xiao, Shiqiang Li, et al.Molecular Vision|October 19, 2012
Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathyHuiqin Yang, Shiqiang Li, Xueshan Xiao, et al.Genes|June 28, 2023
Non-Pharmaceutical Interventions against COVID-19 Causing a Lower Trend in Age of LHON OnsetYuxi Zheng, Xiaoyun Jia, Shiqiang Li, et al.Molecular Vision|July 19, 2008
Evaluation of EGR1 as a candidate gene for high myopiaTuo Li, Xueshan Xiao, Shiqiang Li, et al.Molecular Vision|February 26, 2021
Confirming and expanding the phenotypes of <i>FZD5</i> variants: Coloboma, inferior chorioretinal hypoplasia, and high myopiaYi Jiang, Jiamin Ouyang, Shiqiang Li, et al.Investigative Ophthalmology & Visual Science|August 16, 2012
PAX6 mutations identified in 4 of 35 families with microcorneaPanfeng Wang, Wenmin Sun, Shiqiang Li, et al.Pageof 17