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

por Li, Liang-Mao, Zhao, Li-Quan, Qu, Ling-Hui, Li, Peng
Publicado 2014

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

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

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

por Qu, Ling-hui, Jin, Xin, Li, Liang-mao, Li, Shi-ying, Xie, Han-ping
Publicado 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

por Zhai, Wei, Jin, Xin, Gong, Yan, Qu, Ling-Hui, Zhao, Chen, Li, Zhao-Hui
Publicado en Int J Ophthalmol (2015)

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

por Qu, Ling-hui, Jin, Xin, Zeng, Chao, Zhou, Nian-gou, Liu, Yan-hong, Lin, Ye
Publicado en Biosci Rep (2021)

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

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

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

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

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

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

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

por 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
Publicado en Stem Cell Res Ther (2017)

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

por 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
Publicado en Biosci Rep (2020)