Showing results (151-160 of 167) with videos related to

Sort By:
Pageof 17
Human Genetics|June 19, 2014
Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencingYan Xu, Liping Guan, Tao Shen, et al.
Investigative Ophthalmology & Visual Science|January 8, 2024
Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 FamiliesDongwei Guo, Shiqiang Li, Xueshan Xiao, et al.
Experimental Eye Research|June 21, 2020
Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosaXing Liu, Jiali Li, Shufen Lin, et al.
Molecular Vision|April 9, 2026
Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndromeDi Zhu, Yuxi Zheng, Yi Jiang, et al.
Brain : a Journal of Neurology|October 18, 2024
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genesYuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
Zoological Research|January 6, 2026
ARR3 variant-induced cone mosaicism alters cone subtype composition and disrupts phototransductionJiamin Ouyang, Zhen Yi, Yi Jiang, et al.
Biomaterials|July 5, 2016
808 nm-excited upconversion nanoprobes with low heating effect for targeted magnetic resonance imaging and high-efficacy photodynamic therapy in HER2-overexpressed breast cancerLeyong Zeng, Yuanwei Pan, Ruifen Zou, et al.
Human Genetics|September 21, 2022
Truncation mutations in MYRF underlie primary angle closure glaucomaJiamin Ouyang, Wenmin Sun, Huangxuan Shen, et al.
Investigative Ophthalmology & Visual Science|March 14, 2023
The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High MyopiaYi Jiang, Lin Zhou, Yingwei Wang, et al.
The British Journal of Ophthalmology|May 15, 2024
Clinical features of patients with mutations in genes for nanophthalmosXueqing Li, Hui Xiao, Yihua Su, et al.
Pageof 17