Showing results (101-110 of 167) with videos related to
Sort By:
Pageof 17
Molecular Vision|July 9, 2016
Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndromeXun Wang, Xiaoyun Jia, Xueshan Xiao, et al.Investigative Ophthalmology & Visual Science|March 9, 2023
Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD SyndromePanfeng Wang, Pengsen Wu, Junwen Wang, et al.Current Eye Research|April 11, 2024
Datasets-Based IMPDH1 Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-PathogenicJunwen Wang, Yingwei Wang, Yi Jiang, et al.Journal of Genetics|March 25, 2021
DNAH17 is essential for rat spermatogenesis and fertilityLiling Chen, Jiamin Ouyang, Xueqing Li, et al.Experimental Eye Research|May 28, 2021
Novel variants in GUCY2D causing retinopathy and the genotype-phenotype correlationZhen Yi, Wenmin Sun, Xueshan Xiao, et al.Frontiers in Immunology|September 15, 2023
Retinopathy as an initial sign of hereditary immunological diseases: report of six families and challenges in eye clinicYingwei Wang, Yi Jiang, Junwen Wang, et al.Molecular Vision|August 19, 2011
Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIPXueshan Xiao, Wei Li, Panfeng Wang, et al.Translational Vision Science & Technology|March 27, 2026
Clinical and Genetic Characteristics of a Chinese Occult Maculopathy CohortZixuan Jiang, Jiamin Ouyang, Zhen Yi, et al.Journal of Translational Medicine|January 19, 2024
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopiaYi Jiang, Xueshan Xiao, Wenmin Sun, et al.Plos One|May 24, 2011
Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosisLin Li, Xueshan Xiao, Shiqiang Li, et al.Pageof 17