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Molecular Vision|September 11, 2020
Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testingWenmin Sun, Shiqiang Li, Xueshan Xiao, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|March 21, 2020
A novel deep intronic COL2A1 mutation in a family with early-onset high myopia/ocular-only Stickler syndromeWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Journal of Human Genetics|September 15, 2006
Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathyXiaoyun Jia, Shiqiang Li, Xueshan Xiao, et al.
Current Eye Research|May 9, 2012
Screening for NDP mutations in 44 unrelated patients with familial exudative vitreoretinopathy or Norrie diseaseHuiqin Yang, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|August 26, 2011
Mutation analysis of 12 genes in Chinese families with congenital cataractsWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Journal of Human Genetics|March 14, 2007
Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1Qingjiong Zhang, Shiqiang Li, Xueshan Xiao, et al.
Biochemical and Biophysical Research Communications|September 14, 2010
Mutation spectrum and frequency of the RHO gene in 248 Chinese families with retinitis pigmentosaShiqiang Li, Xueshan Xiao, Panfeng Wang, et al.
Molecular Vision|November 11, 2016
X-linked heterozygous mutations in <i>ARR3</i> cause female-limited early onset high myopiaXueshan Xiao, Shiqiang Li, Xiaoyun Jia, et al.
Molecular Vision|May 10, 2011
Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypesHuiqin Yang, Xueshan Xiao, Shiqiang Li, et al.
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