Kết quả tìm kiếm - Wu, Qingxiu

Retro-orbital injection of FITC-dextran combined with isolectin B4 in assessing the retinal neovascularization defect Bằng Li, Jizhu, Wu, Yuqing, Liu, Bingqian, Huang, Ying, Wu, Qingxiu, Li, Haichun, Xiao, Sainan, Lin, Ying, Li, Tao

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Influence of NQO1 Polymorphisms on Warfarin Maintenance Dose: A Systematic Review and Meta-Analysis (rs1800566 and rs10517) Bằng Tian, Lihong, Xiao, Pingping, Zhou, Bingrong, Chen, Yishan, Kang, Lijuan, Wang, Qingqing, Lin, Jianfeng, Son, Min, Wu, Qingxiu

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Multimodal imaging and genetic analysis of adult-onset best vitelliform macular dystrophy in Chinese patients Bằng Lin, Ying, Li, Tao, Liu, Bingqian, Lyu, Cancan, Lian, Yu, Li, Jizhu, Huang, Ying, Li, Haichun, Wu, Qingxiu, Jin, Chenjin, Lu, Lin

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Targeted next-generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment Bằng Huang, Xinhua, Lin, Ying, Chen, Chuan, Zhu, Yi, Gao, Hongbin, Li, Tao, Liu, Bingqian, Lyu, Cancan, Huang, Ying, Wu, Qingxiu, Li, Haichun, Jin, Chenjin, Liang, Xiaoling, Lu, Lin

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Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract Bằng Lin, Ying, Gao, Hongbin, Zhu, Yi, Chen, Chuan, Li, Tao, Liu, Bingqian, Lyu, Cancan, Huang, Ying, Li, Haichun, Wu, Qingxiu, Jin, Chenjin, Liang, Xiaoling, Huang, Xinhua, Lu, Lin

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Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma Bằng Li, Tao, Lin, Ying, Gao, Hongbin, Chen, Chuan, Zhu, Yi, Liu, Bingqian, Lian, Yu, Li, Yonghao, Zhou, Wenli, Jiang, Hongye, Li, Haichun, Wu, Qingxiu, Liang, Xiaoling, Jin, Chenjin, Huang, Xinhua, Lu, Lin

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Genetic variations in Bestrophin-1 and associated clinical findings in two Chinese patients with juvenile-onset and adult-onset best vitelliform macular dystrophy Bằng Lin, Ying, Li, Tao, Ma, Chenghong, Gao, Hongbin, Chen, Chuan, Zhu, Yi, Liu, Bingqian, Lian, Yu, Huang, Ying, Li, Haichun, Wu, Qingxiu, Liang, Xiaoling, Jin, Chenjin, Huang, Xinhua, Ye, Jianhua, Lu, Lin

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Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy Bằng Lin, Ying, Gao, Hongbin, Chen, Chuan, Zhu, Yi, Li, Tao, Liu, Bingqian, Ma, Chenghong, Jiang, Hongye, Li, Yonghao, Huang, Ying, Wu, Qingxiu, Li, Haichun, Liang, Xiaoling, Jin, Chenjin, Ye, Jianhua, Huang, Xinhua, Lu, Lin

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FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome Bằng Lin, Ying, Gao, Hongbin, Ai, Siming, Eswarakumar, Jacob V.P., Zhu, Yi, Chen, Chuan, Li, Tao, Liu, Bingqian, Jiang, Hongye, Liu, Yuhua, Li, Yonghao, Wu, Qingxiu, Li, Haichun, Liang, Xiaoling, Jin, Chenjin, Huang, Xinhua, Lu, Lin

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