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Showing results (601-610 of 763) with videos related to

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G3 (Bethesda, Md.)|August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern AustraliaShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Investigative Ophthalmology & Visual Science|June 15, 2022
Axial Length Distributions in Patients With Genetically Confirmed Inherited Retinal DiseasesKatie M Williams, Michalis Georgiou, Angelos Kalitzeos, et al.
American Journal of Human Genetics|October 20, 2021
Establishing risk of vision loss in Leber hereditary optic neuropathyM Isabel G Lopez Sanchez, Lisa S Kearns, Sandra E Staffieri, et al.
Human Genetics|August 29, 2009
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesDavid P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Investigative Ophthalmology & Visual Science|March 28, 2009
An international collaborative family-based whole-genome linkage scan for high-grade myopiaYi-Ju Li, Jeremy A Guggenheim, Anuradha Bulusu, et al.
European Journal of Medical Genetics|June 13, 2017
Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutationsMark A Corbett, Samantha J Turner, Alison Gardner, et al.
BMJ Open Ophthalmology|September 26, 2022
Pathogenic genetic variants identified in Australian families with paediatric cataractJohanna L Jones, Bennet J McComish, Sandra E Staffieri, et al.
American Journal of Ophthalmology|November 5, 2003
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucomaWallace L M Alward, Young H Kwon, Kazuhide Kawase, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variabilityMichael B Petersen, George Kitsos, John R Samples, et al.
Psychosomatic Medicine|November 7, 2014
Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adultsMadeline H Meier, Nathan A Gillespie, Narelle K Hansell, et al.
Pageof 77

Showing results (601-610 of 763) with videos related to

Sort By:
Pageof 77
G3 (Bethesda, Md.)|August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern AustraliaShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Investigative Ophthalmology & Visual Science|June 15, 2022
Axial Length Distributions in Patients With Genetically Confirmed Inherited Retinal DiseasesKatie M Williams, Michalis Georgiou, Angelos Kalitzeos, et al.
American Journal of Human Genetics|October 20, 2021
Establishing risk of vision loss in Leber hereditary optic neuropathyM Isabel G Lopez Sanchez, Lisa S Kearns, Sandra E Staffieri, et al.
Human Genetics|August 29, 2009
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesDavid P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Investigative Ophthalmology & Visual Science|March 28, 2009
An international collaborative family-based whole-genome linkage scan for high-grade myopiaYi-Ju Li, Jeremy A Guggenheim, Anuradha Bulusu, et al.
European Journal of Medical Genetics|June 13, 2017
Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutationsMark A Corbett, Samantha J Turner, Alison Gardner, et al.
BMJ Open Ophthalmology|September 26, 2022
Pathogenic genetic variants identified in Australian families with paediatric cataractJohanna L Jones, Bennet J McComish, Sandra E Staffieri, et al.
American Journal of Ophthalmology|November 5, 2003
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucomaWallace L M Alward, Young H Kwon, Kazuhide Kawase, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variabilityMichael B Petersen, George Kitsos, John R Samples, et al.
Psychosomatic Medicine|November 7, 2014
Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adultsMadeline H Meier, Nathan A Gillespie, Narelle K Hansell, et al.
Pageof 77