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Frontiers in Immunology
|
September 15, 2023
Retinopathy as an initial sign of hereditary immunological diseases: report of six families and challenges in eye clinic
Yingwei Wang, Yi Jiang, Junwen Wang, et al.
Molecular Vision
|
August 19, 2011
Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP
Xueshan Xiao, Wei Li, Panfeng Wang, et al.
Current Eye Research
|
April 11, 2024
Datasets-Based <i>IMPDH1</i> Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-Pathogenic
Junwen Wang, Yingwei Wang, Yi Jiang, et al.
Wei Sheng Yan Jiu = Journal of Hygiene Research
|
September 23, 2024
[Correlation between triglyceride glucose product index and food intake and type 2 diabetes]
Junjun Zhou, Weimin Kong, Jin Chen, et al.
Translational Vision Science & Technology
|
March 27, 2026
Clinical and Genetic Characteristics of a Chinese Occult Maculopathy Cohort
Zixuan Jiang, Jiamin Ouyang, Zhen Yi, et al.
Journal of Genetics
|
March 25, 2021
<i>DNAH17</i> is essential for rat spermatogenesis and fertility
Liling Chen, Jiamin Ouyang, Xueqing Li, et al.
Experimental Eye Research
|
May 28, 2021
Novel variants in GUCY2D causing retinopathy and the genotype-phenotype correlation
Zhen Yi, Wenmin Sun, Xueshan Xiao, et al.
Journal of Translational Medicine
|
January 19, 2024
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia
Yi Jiang, Xueshan Xiao, Wenmin Sun, et al.
Experimental Eye Research
|
March 20, 2016
Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands
Li Huang, Xueshan Xiao, Shiqiang Li, et al.
Neuroscience Letters
|
February 23, 2013
Novel GUCA1A mutation identified in a Chinese family with cone-rod dystrophy
Li Huang, Shiqiang Li, Xueshan Xiao, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 95) with videos related to
Sort By:
Page
of 10
Frontiers in Immunology
|
September 15, 2023
Retinopathy as an initial sign of hereditary immunological diseases: report of six families and challenges in eye clinic
Yingwei Wang, Yi Jiang, Junwen Wang, et al.
Molecular Vision
|
August 19, 2011
Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP
Xueshan Xiao, Wei Li, Panfeng Wang, et al.
Current Eye Research
|
April 11, 2024
Datasets-Based <i>IMPDH1</i> Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-Pathogenic
Junwen Wang, Yingwei Wang, Yi Jiang, et al.
Wei Sheng Yan Jiu = Journal of Hygiene Research
|
September 23, 2024
[Correlation between triglyceride glucose product index and food intake and type 2 diabetes]
Junjun Zhou, Weimin Kong, Jin Chen, et al.
Translational Vision Science & Technology
|
March 27, 2026
Clinical and Genetic Characteristics of a Chinese Occult Maculopathy Cohort
Zixuan Jiang, Jiamin Ouyang, Zhen Yi, et al.
Journal of Genetics
|
March 25, 2021
<i>DNAH17</i> is essential for rat spermatogenesis and fertility
Liling Chen, Jiamin Ouyang, Xueqing Li, et al.
Experimental Eye Research
|
May 28, 2021
Novel variants in GUCY2D causing retinopathy and the genotype-phenotype correlation
Zhen Yi, Wenmin Sun, Xueshan Xiao, et al.
Journal of Translational Medicine
|
January 19, 2024
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia
Yi Jiang, Xueshan Xiao, Wenmin Sun, et al.
Experimental Eye Research
|
March 20, 2016
Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands
Li Huang, Xueshan Xiao, Shiqiang Li, et al.
Neuroscience Letters
|
February 23, 2013
Novel GUCA1A mutation identified in a Chinese family with cone-rod dystrophy
Li Huang, Shiqiang Li, Xueshan Xiao, et al.
Page
of 10