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International Journal of Molecular Medicine|February 19, 2014
Detection of CRB1 mutations in families with retinal dystrophy through phenotype-oriented mutational screeningShiqiang Li, Tao Shen, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|January 26, 2007
The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individualsQingjiong Zhang, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|June 21, 2011
Mutational screening of six genes in Chinese patients with congenital cataract and microcorneaWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Plos One|June 27, 2014
Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS geneWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 20, 2021
Genotype-Phenotype of Isolated Foveal Hypoplasia in a Large Cohort: Minor Iris Changes as an Indicator of PAX6 InvolvementYi Jiang, Shiqiang Li, Xueshan Xiao, et al.
Biochemical and Biophysical Research Communications|November 16, 2010
mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese populationXiaoyun Jia, Shiqiang Li, Panfeng Wang, et al.
International Journal of Molecular Medicine|June 28, 2012
Mutation screening of TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindnessQin Wang, Yang Gao, Shiqiang Li, et al.
Analytica Chimica Acta|April 18, 2024
Confined DNA tetrahedral molecular sieve for size-selective electrochemiluminescence sensingShiqiang Li, Mingyu Leng, Zongbing Li, et al.
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