Search Results - Wu, Qingxiu

  • Showing 1 - 9 results of 9
Refine Results
  1. 1
    Retro-orbital injection of FITC-dextran combined with isolectin B4 in assessing the retinal neovascularization defect

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

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  2. 2
    Influence of NQO1 Polymorphisms on Warfarin Maintenance Dose: A Systematic Review and Meta-Analysis (rs1800566 and rs10517)

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

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  3. 3
    Multimodal imaging and genetic analysis of adult-onset best vitelliform macular dystrophy in Chinese patients

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

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  4. 4
    Targeted next-generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment

    Targeted next-generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment by 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

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  5. 5
    Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract

    Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract by 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

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  6. 6
    Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma

    Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma by 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

    Published 2017
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  7. 7
    Genetic variations in Bestrophin-1 and associated clinical findings in two Chinese patients with juvenile-onset and adult-onset best vitelliform macular dystrophy

    Genetic variations in Bestrophin-1 and associated clinical findings in two Chinese patients with juvenile-onset and adult-onset best vitelliform macular dystrophy by 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

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  8. 8
    Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy

    Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy by 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

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  9. 9
    FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome

    FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome by 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

    Published 2017
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: