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Qingjiong Zhang

Showing results (1-10 of 232) with videos related to

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Progress in Molecular Biology and Translational Science|August 28, 2015
Genetics of Refraction and MyopiaQingjiong Zhang
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|August 5, 2016
Retinitis Pigmentosa: Progress and PerspectiveQingjiong Zhang
Molecular Vision|February 2, 2018
Insight into the molecular genetics of myopiaJiali Li, Qingjiong Zhang
Ophthalmic Genetics|April 10, 2020
Heterozygous structural variation mimicking homozygous missense mutations in NEU1 associated with presenting clinical signs in eyes aloneXueqing Li, Qingjiong Zhang
American Journal of Medical Genetics. Part A|July 18, 2009
Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutationXueshan Xiao, 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
American Journal of Medical Genetics. Part A|July 17, 2023
A case of LSS-associated congenital nuclear cataract with hypotrichosis and literature reviewDongwei Guo, Qingjiong Zhang
Yan Ke Xue Bao = Eye Science|October 30, 2004
[Transcription changes of alpha A-crystallins gene during the development of retinal degeneration in Rd, Rds and C3H mouse]Dajiang Li, Qingjiong Zhang
Ophthalmic Genetics|December 17, 2011
Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutationXueshan Xiao, Shiqiang Li, Qingjiong Zhang
Molecular Vision|February 6, 2007
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndromeJuan Wang, Jinling Liu, Qingjiong Zhang
Pageof 24

Showing results (1-10 of 232) with videos related to

Sort By:
Pageof 24
Progress in Molecular Biology and Translational Science|August 28, 2015
Genetics of Refraction and MyopiaQingjiong Zhang
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|August 5, 2016
Retinitis Pigmentosa: Progress and PerspectiveQingjiong Zhang
Molecular Vision|February 2, 2018
Insight into the molecular genetics of myopiaJiali Li, Qingjiong Zhang
Ophthalmic Genetics|April 10, 2020
Heterozygous structural variation mimicking homozygous missense mutations in NEU1 associated with presenting clinical signs in eyes aloneXueqing Li, Qingjiong Zhang
American Journal of Medical Genetics. Part A|July 18, 2009
Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutationXueshan Xiao, 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
American Journal of Medical Genetics. Part A|July 17, 2023
A case of LSS-associated congenital nuclear cataract with hypotrichosis and literature reviewDongwei Guo, Qingjiong Zhang
Yan Ke Xue Bao = Eye Science|October 30, 2004
[Transcription changes of alpha A-crystallins gene during the development of retinal degeneration in Rd, Rds and C3H mouse]Dajiang Li, Qingjiong Zhang
Ophthalmic Genetics|December 17, 2011
Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutationXueshan Xiao, Shiqiang Li, Qingjiong Zhang
Molecular Vision|February 6, 2007
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndromeJuan Wang, Jinling Liu, Qingjiong Zhang
Pageof 24