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The British Journal of Ophthalmology|October 17, 2015
KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathyHuan Hu, Xueshan Xiao, Shiqiang Li, et al.JAMA Ophthalmology|June 7, 2014
Identification of CNGA3 mutations in 46 families: common cause of achromatopsia and cone-rod dystrophies in Chinese patientsShiqiang Li, Li Huang, Xueshan Xiao, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|April 1, 2021
Systemic Genotype-Phenotype Analysis of MYOC Variants Based on Exome Sequencing and Literature ReviewXueqing Li, Xueshan Xiao, Shiqiang Li, et al.Molecular Vision|January 6, 2012
Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutationsLin Li, Xueshan Xiao, Shiqiang Li, et al.Molecular Vision|July 30, 2005
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612Qingjiong Zhang, Xiangming Guo, Xueshan Xiao, et al.Investigative Ophthalmology & Visual Science|January 14, 2026
Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature ReviewShu Liu, Shiqiang Li, Yingwei Wang, et al.International Journal of Molecular Medicine|January 17, 2012
Novel RS1 mutations associated with X-linked juvenile retinoschisisJunhui Yi, Shiqiang Li, Xiaoyun Jia, et al.Current Topics in Microbiology and Immunology|July 20, 2020
Advances in Development of mRNA-Based TherapeuticsLei Huang, Luyao Zhang, Weiwei Li, et al.Neuroscience Letters|August 14, 2020
Feasibility of commonly used fluorescent dyes and viral tracers in aqueous and solvent-based tissue clearingPeixin Wang, Dan Zhang, Shaocong Bai, et al.Molecular Vision|May 26, 2021
Heterozygous <i>GJA1</i> variants with ocular phenotype: Missense in domain but truncation out of domainXueqing Li, Xueshan Xiao, Shiqiang Li, et al.Pageof 22