检索结果 - Wu, Qingxiu

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