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Inorganic Chemistry|April 7, 2020
Discovery of a Fullerene-Polyoxometalate Hybrid Exhibiting Enhanced Photocurrent ResponseWeidong Yu, Bin Li, Yin Zhang, et al.Plos One|January 13, 2017
Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic NeuropathyYadi Li, Jie Li, Xiaoyun Jia, et al.Molecular Medicine Reports|March 25, 2017
GPR143 mutations in Chinese patients with ocular albinism type 1Xiuhua Jia, Jin Yuan, Xiaoyun Jia, et al.Molecular Vision|August 19, 2011
Mutation spectrum of PAX6 in Chinese patients with aniridiaXiaohui Zhang, Panfeng Wang, Shiqiang Li, et al.Molecular Medicine Reports|June 29, 2017
Novel mutations of FRMD7 in Chinese patients with congenital motor nystagmusXiuhua Jia, Xiang Zhu, Qigen Li, et al.Journal of Human Genetics|October 22, 2005
Linkage analysis of two families with X-linked recessive congenital motor nystagmusXiangming Guo, Shiqiang Li, Xiaoyun Jia, et al.The British Journal of Ophthalmology|October 17, 2015
KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathyHuan Hu, Xueshan Xiao, Shiqiang Li, et al.JAMA Ophthalmology|June 7, 2014
Identification of CNGA3 mutations in 46 families: common cause of achromatopsia and cone-rod dystrophies in Chinese patientsShiqiang Li, Li Huang, Xueshan Xiao, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|April 1, 2021
Systemic Genotype-Phenotype Analysis of MYOC Variants Based on Exome Sequencing and Literature ReviewXueqing Li, Xueshan Xiao, Shiqiang Li, et al.Journal of Robotic Surgery|September 5, 2025
Interpretable machine learning model predicts 1-year inguinal hernia risk after robot-assisted radical prostatectomyWeidong Yu, You Ma, Junchao Wu, et al.Pageof 171