Výsledky vyhledávání - Wu, Qingxiu

Retro-orbital injection of FITC-dextran combined with isolectin B4 in assessing the retinal neovascularization defect Autor 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) Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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