Excimer Laser Phototherapeutic Keratectomy for the Treatment of Clinically Presumed Fungal Keratitis

द्वारा Li, Liang-Mao, Zhao, Li-Quan, Qu, Ling-Hui, Li, Peng
प्रकाशित 2014

Detecting genetic variations in hereditary retinal dystrophies with next-generation sequencing technology

द्वारा Jin, Xin, Qu, Ling Hui, Meng, Xiao Hong, Xu, Hai Wei, Yin, Zheng Qin
प्रकाशित 2014

A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

द्वारा Qu, Ling-hui, Jin, Xin, Li, Liang-mao, Li, Shi-ying, Xie, Han-ping
प्रकाशित 2014

Phenotype of Usher syndrome type II assosiated with compound missense mutations of c.721 C>T and c.1969 C>T in MYO7A in a Chinese Usher syndrome family

द्वारा Zhai, Wei, Jin, Xin, Gong, Yan, Qu, Ling-Hui, Zhao, Chen, Li, Zhao-Hui
में प्रकाशित Int J Ophthalmol (2015)

Targeted next-generation sequencing identifies ABCA4 mutations in Chinese families with childhood-onset and adult-onset Stargardt disease

द्वारा Qu, Ling-hui, Jin, Xin, Zeng, Chao, Zhou, Nian-gou, Liu, Yan-hong, Lin, Ye
में प्रकाशित Biosci Rep (2021)

Haplotype Analysis of Association of the MYOC Gene with Primary Angle-Closure Glaucoma in a Han Chinese Population

द्वारा Jin, Xin, Wang, Da-Jiang, Qu, Ling-Hui, Hou, Bao-Ke, Gong, Yan, Xu, Wei-Wei
में प्रकाशित Genet Test Mol Biomarkers (2015)

Correction: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

द्वारा Qu, Ling-hui, Jin, Xin, Li, Liang-mao, Li, Shi-ying, Yin, Zheng-qin, Xie, Han-ping
प्रकाशित 2014

Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family

द्वारा Jin, Xin, Qu, Ling-Hui, Hou, Bao-Ke, Xu, Hai-Wei, Meng, Xiao-Hong, Pang, Chi-Pui, Yin, Zheng-Qin
में प्रकाशित Biosci Rep (2016)

Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients

द्वारा Liu, Yong, Chen, Shao Jun, Li, Shi Ying, Qu, Ling Hui, Meng, Xiao Hong, Wang, Yi, Xu, Hai Wei, Liang, Zhi Qing, Yin, Zheng Qin
में प्रकाशित Stem Cell Res Ther (2017)

Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing

द्वारा Qu, Ling-hui, Jin, Xin, Long, Yan-ling, Ren, Jia-yun, Weng, Chuang-huang, Xu, Hai-wei, Liu, Yong, Meng, Xiao-hong, Li, Shi-ying, Yin, Zheng-qin
में प्रकाशित Biosci Rep (2020)