Retinal displacement after closure of idiopathic macular hole by Zhong-Cui Sun, Min Wang, Jia-Wen Fan, Ge-Zhi Xu

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Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family by Yu-He Qi, Feng-Juan Gao, Fang-Yuan Hu, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Jun-Yi Chen, Wan-Jing Huang, Guo-Hong Tian, Min Wang, De-Kang Gan, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu

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A simple new technique for the induction of residual posterior vitreous cortex removal and membrane peeling by Wen-Yi Tang, Ting Zhang, Ke-Yan Wang, Qing Chang, Xin Huang, Ge-Zhi Xu

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Effect of Phosphorylated-Extracellular Regulated Kinase 1/2 Inhibitor on Retina from Light-induced Photoreceptor Degeneration by Xin-Yi Ding, Rui-Ping Gu, Wen-Yi Tang, Qin-Meng Shu, Ge-Zhi Xu, Meng Zhang

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Focal choroidal excavation complicated with choroidal neovascularization in young and middle aged patients by Wen-Yi Tang, Ting Zhang, Qin-Meng Shu, Chun-Hui Jiang, Qing Chang, Hong Zhuang, Ge-Zhi Xu

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Pediatric Infectious Endophthalmitis: A 271-case Retrospective Study at a Single Center in China by Meng Zhang, Ge-Zhi Xu, Rui Jiang, Ying-Qin Ni, Ke-Yan Wang, Rui-Ping Gu, Xin-Yi Ding

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Mutation Analysis of the RPGR Gene in a Chinese Cohort by Hong-Li Liu, Hong-Li Liu, Hong-Li Liu, Hong-Li Liu, Feng-Guan Gao, Feng-Guan Gao, Feng-Guan Gao, Feng-Guan Gao, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Ping Xu, Ping Xu, Ping Xu, Ping Xu, Qing Chang, Qing Chang, Qing Chang, Qing Chang, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu

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Downregulation of circRNA DMNT3B contributes to diabetic retinal vascular dysfunction through targeting miR-20b-5p and BAMBI by Ke Zhu, Xin Hu, Han Chen, Fang Li, Ning Yin, Ai-Lin Liu, Kun Shan, Yao-Wu Qin, Xin Huang, Qing Chang, Ge-Zhi Xu, Zhongfeng Wang

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Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses by Feng-Juan Gao, Guo-Hong Tian, Fang-Yuan Hu, Dan-Dan Wang, Jian-Kang Li, Qing Chang, Fang Chen, Ge-Zhi Xu, Wei Liu, Ji-Hong Wu

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ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants by Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Jian-kang Li, Jian-kang Li, Feng-Juan Gao, Feng-Juan Gao, Feng-Juan Gao, Feng-Juan Gao, Yu-He Qi, Yu-He Qi, Yu-He Qi, Yu-He Qi, Ping Xu, Ping Xu, Ping Xu, Ping Xu, Yong-Jin Zhang, Yong-Jin Zhang, Yong-Jin Zhang, Yong-Jin Zhang, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Lu-Sheng Wang, Wei Li, Wei Li, Min Wang, Min Wang, Min Wang, Min Wang, Fang Chen, Fang Chen, Fang Chen, Si-Mai Shen, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Qing Chang, Qing Chang, Qing Chang, Qing Chang, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu

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Expanding the clinical and genetic spectrum of Heimler syndrome by Feng-Juan Gao, Fang-Yuan Hu, Ping Xu, Yu-He Qi, Jian-Kang Li, Yong-Jin Zhang, Fang Chen, Qing Chang, Fang Song, Si-Mai Shen, Ge-Zhi Xu, Ji-Hong Wu

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