Hasil Pencarian - Ge-Zhi Xu
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Retinal displacement after closure of idiopathic macular hole oleh Zhong-Cui Sun, Min Wang, Jia-Wen Fan, Ge-Zhi Xu
Diterbitkan 2018-01-01
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Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family oleh 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
Diterbitkan 2017-08-01
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A simple new technique for the induction of residual posterior vitreous cortex removal and membrane peeling oleh Wen-Yi Tang, Ting Zhang, Ke-Yan Wang, Qing Chang, Xin Huang, Ge-Zhi Xu
Diterbitkan 2021-04-01
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Pediatric Infectious Endophthalmitis: A 271-case Retrospective Study at a Single Center in China oleh Meng Zhang, Ge-Zhi Xu, Rui Jiang, Ying-Qin Ni, Ke-Yan Wang, Rui-Ping Gu, Xin-Yi Ding
Diterbitkan 2016-01-01
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Mutation Analysis of the RPGR Gene in a Chinese Cohort oleh 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
Diterbitkan 2022-03-01
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Downregulation of circRNA DMNT3B contributes to diabetic retinal vascular dysfunction through targeting miR-20b-5p and BAMBI oleh 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
Diterbitkan 2019-11-01
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Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses oleh 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
Diterbitkan 2020-06-01
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ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants oleh 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
Diterbitkan 2019-09-01
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Expanding the clinical and genetic spectrum of Heimler syndrome oleh 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
Diterbitkan 2019-12-01
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Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population oleh Feng-Juan Gao, Dan-Dan Wang, Jian-Kang Li, Fang-Yuan Hu, Ping Xu, Fang Chen, Yu-He Qi, Wei Liu, Wei Li, Sheng-Hai Zhang, Qing Chang, Ge-Zhi Xu, Ji-Hong Wu
Diterbitkan 2021-04-01
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