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G Robson

Showing results (381-390 of 456) with videos related to

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American Journal of Ophthalmology|November 17, 2023
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female CarriersMichalis Georgiou, Anthony G Robson, Sami H Uwaydat, et al.
Investigative Ophthalmology & Visual Science|December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive InheritanceNeringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
The British Journal of Ophthalmology|October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1Robert H Henderson, Donna S Mackay, Zheng Li, et al.
Investigative Ophthalmology & Visual Science|June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night BlindnessRola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, et al.
Advanced Materials (Deerfield Beach, Fla.)|October 11, 2021
Deterministic Shallow Dopant Implantation in Silicon with Detection Confidence Upper-Bound to 99.85% by Ion-Solid InteractionsAlexander M Jakob, Simon G Robson, Vivien Schmitt, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, et al.
Investigative Ophthalmology & Visual Science|April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher SyndromeJuan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
Investigative Ophthalmology & Visual Science|November 12, 2024
The Electroretinogram I-Wave, a Component Originating in the Retinal OFF-Pathway, Associates With a Myopia Genetic Risk PolymorphismZihe Xu, Jit Kai Tan, Krishnika Vetrivel, et al.
Acta Ophthalmologica|January 1, 2019
Unilateral pigmentary retinopathy: a retrospective case seriesMarie-Hélène Errera, Anthony G Robson, Tracey Wong, et al.
Journal of Medical Genetics|July 10, 2008
ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicingR Burgess, R E MacLaren, A E Davidson, et al.
Pageof 46

Showing results (381-390 of 456) with videos related to

Sort By:
Pageof 46
American Journal of Ophthalmology|November 17, 2023
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female CarriersMichalis Georgiou, Anthony G Robson, Sami H Uwaydat, et al.
Investigative Ophthalmology & Visual Science|December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive InheritanceNeringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
The British Journal of Ophthalmology|October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1Robert H Henderson, Donna S Mackay, Zheng Li, et al.
Investigative Ophthalmology & Visual Science|June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night BlindnessRola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, et al.
Advanced Materials (Deerfield Beach, Fla.)|October 11, 2021
Deterministic Shallow Dopant Implantation in Silicon with Detection Confidence Upper-Bound to 99.85% by Ion-Solid InteractionsAlexander M Jakob, Simon G Robson, Vivien Schmitt, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, et al.
Investigative Ophthalmology & Visual Science|April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher SyndromeJuan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
Investigative Ophthalmology & Visual Science|November 12, 2024
The Electroretinogram I-Wave, a Component Originating in the Retinal OFF-Pathway, Associates With a Myopia Genetic Risk PolymorphismZihe Xu, Jit Kai Tan, Krishnika Vetrivel, et al.
Acta Ophthalmologica|January 1, 2019
Unilateral pigmentary retinopathy: a retrospective case seriesMarie-Hélène Errera, Anthony G Robson, Tracey Wong, et al.
Journal of Medical Genetics|July 10, 2008
ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicingR Burgess, R E MacLaren, A E Davidson, et al.
Pageof 46