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Wenmin Sun

Showing results (1-10 of 95) with videos related to

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JAMA Ophthalmology|November 28, 2014
Does the association between TMEM98 and nanophthalmos require further confirmation?Wenmin Sun, Qingjiong Zhang
Ophthalmic Genetics|July 31, 2018
A novel variant in IDH3A identified in a case with Leber congenital amaurosis accompanied by macular pseudocolobomaWenmin Sun, Qingjiong Zhang
Progress in Molecular Biology and Translational Science|February 4, 2019
Diseases associated with mutations in CNGA3: Genotype-phenotype correlation and diagnostic guidelineWenmin Sun, Qingjiong Zhang
Current Eye Research|May 20, 2021
Start and End with Genetics: <i>RCBTB1</i> and BeyondJunxing Yang, Wenmin Sun, Qingjiong Zhang
American Journal of Medical Genetics. Part A|August 13, 2019
Correspondence to Rossetti et al.'s review of the phenotypic spectrum associated with haploinsufficiency of MYRFWenmin Sun, Xueshan Xiao, Qingjiong Zhang
Stem Cell Research|June 3, 2023
Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1Zixuan Jiang, Wenmin Sun, Qingjiong Zhang, et al.
Molecular Vision|September 11, 2020
Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testingWenmin Sun, Shiqiang Li, Xueshan Xiao, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|March 21, 2020
A novel deep intronic COL2A1 mutation in a family with early-onset high myopia/ocular-only Stickler syndromeWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|August 26, 2011
Mutation analysis of 12 genes in Chinese families with congenital cataractsWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|June 21, 2011
Mutational screening of six genes in Chinese patients with congenital cataract and microcorneaWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Pageof 10

Showing results (1-10 of 95) with videos related to

Sort By:
Pageof 10
JAMA Ophthalmology|November 28, 2014
Does the association between TMEM98 and nanophthalmos require further confirmation?Wenmin Sun, Qingjiong Zhang
Ophthalmic Genetics|July 31, 2018
A novel variant in IDH3A identified in a case with Leber congenital amaurosis accompanied by macular pseudocolobomaWenmin Sun, Qingjiong Zhang
Progress in Molecular Biology and Translational Science|February 4, 2019
Diseases associated with mutations in CNGA3: Genotype-phenotype correlation and diagnostic guidelineWenmin Sun, Qingjiong Zhang
Current Eye Research|May 20, 2021
Start and End with Genetics: <i>RCBTB1</i> and BeyondJunxing Yang, Wenmin Sun, Qingjiong Zhang
American Journal of Medical Genetics. Part A|August 13, 2019
Correspondence to Rossetti et al.'s review of the phenotypic spectrum associated with haploinsufficiency of MYRFWenmin Sun, Xueshan Xiao, Qingjiong Zhang
Stem Cell Research|June 3, 2023
Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1Zixuan Jiang, Wenmin Sun, Qingjiong Zhang, et al.
Molecular Vision|September 11, 2020
Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testingWenmin Sun, Shiqiang Li, Xueshan Xiao, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|March 21, 2020
A novel deep intronic COL2A1 mutation in a family with early-onset high myopia/ocular-only Stickler syndromeWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|August 26, 2011
Mutation analysis of 12 genes in Chinese families with congenital cataractsWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|June 21, 2011
Mutational screening of six genes in Chinese patients with congenital cataract and microcorneaWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Pageof 10