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

por Li, Jizhu, Wu, Yuqing, Liu, Bingqian, Huang, Ying, Wu, Qingxiu, Li, Haichun, Xiao, Sainan, Lin, Ying, Li, Tao
Publicado 2021

Influence of NQO1 Polymorphisms on Warfarin Maintenance Dose: A Systematic Review and Meta-Analysis (rs1800566 and rs10517)

por Tian, Lihong, Xiao, Pingping, Zhou, Bingrong, Chen, Yishan, Kang, Lijuan, Wang, Qingqing, Lin, Jianfeng, Son, Min, Wu, Qingxiu
Publicado 2021

Multimodal imaging and genetic analysis of adult-onset best vitelliform macular dystrophy in Chinese patients

por Lin, Ying, Li, Tao, Liu, Bingqian, Lyu, Cancan, Lian, Yu, Li, Jizhu, Huang, Ying, Li, Haichun, Wu, Qingxiu, Jin, Chenjin, Lu, Lin
Publicado 2021

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

por 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
Publicado 2018

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

por 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
Publicado 2018

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

por 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
Publicado 2017

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

por 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
Publicado 2018

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

por 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
Publicado 2018

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

por 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
Publicado 2017