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Showing results (871-880 of 1,250) with videos related to

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JMIR Formative Research|January 31, 2022
Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility StudyRose M Gilbert, Dayyanah Sumodhee, Nikolas Pontikos, et al.
Virology Journal|May 5, 2007
Genome-wide diversity and selective pressure in the human rhinovirusAmy L Kistler, Dale R Webster, Silvi Rouskin, et al.
Investigative Ophthalmology & Visual Science|June 27, 2006
Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunctionMichel Michaelides, Sharon A Jenkins, Milam A Brantley, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Molecular Vision|June 19, 2009
Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophyZ Saihan, Z Li, J Rice, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth CohortPirro G Hysi, Claire L Simpson, Yvonne K Y Fok, et al.
The British Journal of Ophthalmology|December 17, 2011
Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2Mala Subash, Tryfonas Rotsos, Genevieve A Wright, et al.
Cells|August 9, 2024
Investigating Splice Defects in <i>USH2A</i> Using Targeted Long-Read SequencingShwetha Chandrasekhar, Siying Lin, Neringa Jurkute, et al.
American Journal of Ophthalmology|July 8, 2023
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher SyndromeMalena Daich Varela, Shiao Wei Wong, Gulunay Kiray, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Pageof 125

Showing results (871-880 of 1,250) with videos related to

Sort By:
Pageof 125
JMIR Formative Research|January 31, 2022
Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility StudyRose M Gilbert, Dayyanah Sumodhee, Nikolas Pontikos, et al.
Virology Journal|May 5, 2007
Genome-wide diversity and selective pressure in the human rhinovirusAmy L Kistler, Dale R Webster, Silvi Rouskin, et al.
Investigative Ophthalmology & Visual Science|June 27, 2006
Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunctionMichel Michaelides, Sharon A Jenkins, Milam A Brantley, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Molecular Vision|June 19, 2009
Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophyZ Saihan, Z Li, J Rice, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth CohortPirro G Hysi, Claire L Simpson, Yvonne K Y Fok, et al.
The British Journal of Ophthalmology|December 17, 2011
Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2Mala Subash, Tryfonas Rotsos, Genevieve A Wright, et al.
Cells|August 9, 2024
Investigating Splice Defects in <i>USH2A</i> Using Targeted Long-Read SequencingShwetha Chandrasekhar, Siying Lin, Neringa Jurkute, et al.
American Journal of Ophthalmology|July 8, 2023
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher SyndromeMalena Daich Varela, Shiao Wei Wong, Gulunay Kiray, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Pageof 125