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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 ARR3 cause female-limited early onset high myopiaXueshan Xiao, Shiqiang Li, Xiaoyun Jia, et al.
Optics Letters|August 14, 2013
Tuning group-velocity dispersion by optical forceWei C Jiang, Qiang Lin
Scientific Reports|November 15, 2016
Chip-scale cavity optomechanics in lithium niobateWei C Jiang, Qiang Lin
World Journal of Gastrointestinal Oncology|June 23, 2025
Prognostic value of post-neoadjuvant immunochemotherapy hypercoagulation in gastric cancer patients undergoing surgeryMeng-Jie Quan, Qiang Lin
Molecular Vision|October 29, 2009
Sequence variations of GRM6 in patients with high myopiaXiaoyu Xu, Shiqiang Li, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|January 15, 2019
Germline Mutations in CTNNB1 Associated With Syndromic FEVR or Norrie DiseaseWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
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