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American Journal of Ophthalmology|December 21, 2020
Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 MutationsYingwei Wang, Wenmin Sun, Xueshan Xiao, et al.Molecular Medicine Reports|April 9, 2013
Screening for variants in 20 genes in 130 unrelated patients with cone-rod dystrophyLi Huang, Shiqiang Li, Xueshan Xiao, et al.The British Journal of Ophthalmology|June 22, 2021
Biallelic variants in <i>CPAMD8</i> are associated with primary open-angle glaucoma and primary angle-closure glaucomaXueqing Li, Wenmin Sun, Xueshan Xiao, et al.Investigative Ophthalmology & Visual Science|December 9, 2008
High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genesPanfeng Wang, Shiqiang Li, Xueshan Xiao, et al.Clinical Genetics|August 22, 2022
Variants in HNRNPH1 are associated with high myopia in humans and ocular coloboma in zebrafishJiamin Ouyang, Shiqiang Li, Wenmin Sun, et al.Applied Optics|October 6, 2021
FMCW lidar multitarget detection based on skeleton tree waveform matchingBingchen Li, Di Mo, Peisi Wang, et al.Organic & Biomolecular Chemistry|September 4, 2023
Effects of phosphine ligands in nickel-catalyzed decarbonylation reactions of lactoneXinghua Wang, Peng Jin, Shiqiang Li, et al.Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|December 14, 2011
Common variants in chromosome 4q25 are associated with myopia in Chinese adultsYang Gao, Panfeng Wang, Shiqiang Li, et al.Nuclear Medicine Communications|April 20, 2005
Radiolabelling of poly(histidine) derivatized biodegradable microspheres with the 188Re tricarbonyl complex [188Re(CO)3(H2O)3]+Junfeng Yu, Urs O Häfeli, Jiaoyun Xia, et al.Human Genetics|April 6, 2020
Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large familiesWenmin Sun, Shiqiang Li, Xiaoyun Jia, et al.Pageof 22