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Lejin Wang

Showing results (1-10 of 24) with videos related to

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Journal of Dermatological Science|August 12, 2009
The first case report of a Chinese Hermansky-Pudlak syndrome patient with a novel mutation on HPS1 geneAihua Wei, Shi Lian, Lejin Wang, et al.
Strabismus|July 11, 2020
Young patients with divergence insufficiency related to excessive near workYu Xia, Liqun Cao, Xiujun Peng, et al.
Indian Journal of Ophthalmology|December 14, 2016
A previously unidentified deletion in G protein-coupled receptor 143 causing X-linked congenital nystagmus in a Chinese familyJing Liu, Yanlei Jia, Lejin Wang, et al.
BMC Ophthalmology|June 26, 2023
Comparing myopic error in patients with basic and convergence insufficiency intermittent exotropia in ChinaQingyu Meng, Lejin Wang, Mingwei Zhao, et al.
Science (New York, N.Y.)|December 3, 2003
Mutation of MEF2A in an inherited disorder with features of coronary artery diseaseLejin Wang, Chun Fan, Sarah E Topol, et al.
Indian Journal of Ophthalmology|July 7, 2016
A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese familyJuan Bu, Sijie He, Lejin Wang, et al.
Circulation|December 15, 2004
Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathyCarlos Oberti, Lejin Wang, Lin Li, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Novel deletion in the pre-mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese familyLejin Wang, Michael Ribaudo, Kanxing Zhao, et al.
Molecular Vision|November 9, 2011
A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese familyWei Du, Juan Bu, Jiamei Dong, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 23, 2002
[A novel rhodopsin E341ter mutation in patients with retinitis pigmentosa and corresponding clinical phenotype]Shihong Xiong, Kanxing Zhao, Li Wang, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Journal of Dermatological Science|August 12, 2009
The first case report of a Chinese Hermansky-Pudlak syndrome patient with a novel mutation on HPS1 geneAihua Wei, Shi Lian, Lejin Wang, et al.
Strabismus|July 11, 2020
Young patients with divergence insufficiency related to excessive near workYu Xia, Liqun Cao, Xiujun Peng, et al.
Indian Journal of Ophthalmology|December 14, 2016
A previously unidentified deletion in G protein-coupled receptor 143 causing X-linked congenital nystagmus in a Chinese familyJing Liu, Yanlei Jia, Lejin Wang, et al.
BMC Ophthalmology|June 26, 2023
Comparing myopic error in patients with basic and convergence insufficiency intermittent exotropia in ChinaQingyu Meng, Lejin Wang, Mingwei Zhao, et al.
Science (New York, N.Y.)|December 3, 2003
Mutation of MEF2A in an inherited disorder with features of coronary artery diseaseLejin Wang, Chun Fan, Sarah E Topol, et al.
Indian Journal of Ophthalmology|July 7, 2016
A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese familyJuan Bu, Sijie He, Lejin Wang, et al.
Circulation|December 15, 2004
Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathyCarlos Oberti, Lejin Wang, Lin Li, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Novel deletion in the pre-mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese familyLejin Wang, Michael Ribaudo, Kanxing Zhao, et al.
Molecular Vision|November 9, 2011
A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese familyWei Du, Juan Bu, Jiamei Dong, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 23, 2002
[A novel rhodopsin E341ter mutation in patients with retinitis pigmentosa and corresponding clinical phenotype]Shihong Xiong, Kanxing Zhao, Li Wang, et al.
Pageof 3