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Wenmin Sun

Showing results (11-20 of 95) with videos related to

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Plos One|June 27, 2014
Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS geneWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 20, 2021
Genotype-Phenotype of Isolated Foveal Hypoplasia in a Large Cohort: Minor Iris Changes as an Indicator of PAX6 InvolvementYi Jiang, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|January 8, 2020
Spectrum, frequency, and genotype-phenotype of mutations in <i>SPATA7</i>Xueshan Xiao, Wenmin Sun, Shiqiang Li, et al.
Experimental Eye Research|October 19, 2019
Pathogenicity discrimination and genetic test reference for CRX variants based on genotype-phenotype analysisZhen Yi, Xueshan Xiao, Shiqiang Li, et al.
Alternative Therapies in Health and Medicine|March 29, 2024
Influence of Dyadic Coping Model on Anxiety and Depression Level and Treatment Compliance in Glaucoma PatientsJinming Cheng, Wenmin Sun, Chaoxia Yu, et al.
Ebiomedicine|March 6, 2022
Corrigendum to "comparative exome sequencing reveals novel candidate genes for retinitis pigmentosa" [EBioMedicine 56(2020)102792] DOI: https://doi.org/10.1016/j.ebiom.2020.102792Zhen Yi, Jiamin Ouyang, Wenmin Sun, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|April 1, 2021
Systemic Genotype-Phenotype Analysis of MYOC Variants Based on Exome Sequencing and Literature ReviewXueqing Li, Xueshan Xiao, Shiqiang Li, et al.
International Journal of Molecular Sciences|April 17, 2025
Clinical and Genetic Characteristics of 18 Patients from Southeast China with ABCA4-Associated Stargardt DiseaseXinyu Liu, Zehao Liu, Jinli Cui, et al.
Current Eye Research|October 26, 2020
Variants in <i>RCBTB1</i> are Associated with Autosomal Recessive Retinitis Pigmentosa but Not Autosomal Dominant FEVRJunxing Yang, Xueshan Xiao, Wenmin Sun, et al.
Investigative Ophthalmology & Visual Science|January 15, 2019
Germline Mutations in CTNNB1 Associated With Syndromic FEVR or Norrie DiseaseWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Pageof 10

Showing results (11-20 of 95) with videos related to

Sort By:
Pageof 10
Plos One|June 27, 2014
Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS geneWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 20, 2021
Genotype-Phenotype of Isolated Foveal Hypoplasia in a Large Cohort: Minor Iris Changes as an Indicator of PAX6 InvolvementYi Jiang, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|January 8, 2020
Spectrum, frequency, and genotype-phenotype of mutations in <i>SPATA7</i>Xueshan Xiao, Wenmin Sun, Shiqiang Li, et al.
Experimental Eye Research|October 19, 2019
Pathogenicity discrimination and genetic test reference for CRX variants based on genotype-phenotype analysisZhen Yi, Xueshan Xiao, Shiqiang Li, et al.
Alternative Therapies in Health and Medicine|March 29, 2024
Influence of Dyadic Coping Model on Anxiety and Depression Level and Treatment Compliance in Glaucoma PatientsJinming Cheng, Wenmin Sun, Chaoxia Yu, et al.
Ebiomedicine|March 6, 2022
Corrigendum to "comparative exome sequencing reveals novel candidate genes for retinitis pigmentosa" [EBioMedicine 56(2020)102792] DOI: https://doi.org/10.1016/j.ebiom.2020.102792Zhen Yi, Jiamin Ouyang, Wenmin Sun, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|April 1, 2021
Systemic Genotype-Phenotype Analysis of MYOC Variants Based on Exome Sequencing and Literature ReviewXueqing Li, Xueshan Xiao, Shiqiang Li, et al.
International Journal of Molecular Sciences|April 17, 2025
Clinical and Genetic Characteristics of 18 Patients from Southeast China with ABCA4-Associated Stargardt DiseaseXinyu Liu, Zehao Liu, Jinli Cui, et al.
Current Eye Research|October 26, 2020
Variants in <i>RCBTB1</i> are Associated with Autosomal Recessive Retinitis Pigmentosa but Not Autosomal Dominant FEVRJunxing Yang, Xueshan Xiao, Wenmin Sun, et al.
Investigative Ophthalmology & Visual Science|January 15, 2019
Germline Mutations in CTNNB1 Associated With Syndromic FEVR or Norrie DiseaseWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
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