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Molecular Vision|February 13, 2013
Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathyYabin Chen, Xiaoyun Jia, Panfeng Wang, et al.
Applied Optics|October 26, 2020
Feature extraction algorithm of precession target based on image length and Doppler broadeningBingchen Li, Di Mo, Ziqi Song, et al.
Experimental Eye Research|December 21, 2020
Spectrum-frequency and genotype-phenotype analysis of rhodopsin variantsHualei Luo, Xueshan Xiao, Shiqiang Li, et al.
Molecular Medicine Reports|September 6, 2012
Evaluation of the ELOVL4, PRPH2 and ABCA4 genes in patients with Stargardt macular degenerationJunhui Yi, Shiqiang Li, Xiaoyun Jia, et al.
American Journal of Medical Genetics. Part A|January 20, 2026
Genetic and Clinical Features of FOXL2-Associated Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Based on 11 Chinese Families and Literature ReviewYijun Dong, Xueshan Xiao, Shiqiang Li, et al.
Frontiers in Genetics|November 8, 2021
Genotype-Phenotype Analysis of <i>RPGR</i> Variations: Reporting of 62 Chinese Families and a Literature ReviewJunxing Yang, Lin Zhou, Jiamin Ouyang, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|November 25, 2010
New reconstruction method of magnetoacoustic tomography with magnetic inductionYang Zhang, Guoqiang Liu, Wenjing He, et al.
IEEE Transactions on Bio-Medical Engineering|September 13, 2021
A Novel Optical Assay System for Bilirubin Concentration Measurement in Whole BloodJean Pierre Ndabakuranye, Anushi E Rajapaksa, Genia Burchall, et al.
Biochemical and Biophysical Research Communications|September 11, 2012
CRX variants in cone-rod dystrophy and mutation overviewLi Huang, Xueshan Xiao, Shiqiang Li, et al.
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