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Molecular Genetics and Genomics : MGG|April 22, 2021
Pathogenicity evaluation and the genotype-phenotype analysis of OPA1 variantsXingyu Xu, Panfeng Wang, Xiaoyun Jia, et al.
Translational Vision Science & Technology|May 21, 2019
An Ophthalmic Targeted Exome Sequencing Panel as a Powerful Tool to Identify Causative Mutations in Patients Suspected of Hereditary Eye DiseasesPanfeng Wang, Shiqiang Li, Wenming Sun, et al.
Molecular Vision|February 28, 2009
Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucomaMei Yang, Xiangming Guo, Xing Liu, et al.
Molecular Vision|November 15, 2013
Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucomaDan Jiang, Zhikuan Yang, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|March 9, 2023
Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD SyndromePanfeng Wang, Pengsen Wu, Junwen Wang, et al.
Translational Vision Science & Technology|March 27, 2026
Clinical and Genetic Characteristics of a Chinese Occult Maculopathy CohortZixuan Jiang, Jiamin Ouyang, Zhen Yi, et al.
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