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Kit Green Sanderson

Showing results (1-10 of 7) with videos related to

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Aesthetic Surgery Journal|June 30, 2019
A Simple Clinical Application for Locating the Frontotemporal Branch of the Facial Nerve Using the Zygomatic Arch and the TragusKit Green Sanderson, Alyssa Conti, Mariah Colussi, et al.
BMJ Case Reports|November 2, 2021
Pigmentary retinopathy masked by asymmetric acquired phenomenaKit Green Sanderson, Kirk A J Stephenson, Adrian Dockery, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 23, 2020
Rod bipolar cell dysfunction in POLG retinopathyKit Green Sanderson, Eoghan Millar, Anupreet Tumber, et al.
BMJ Case Reports|February 10, 2021
Monocular syphilitic uveitisDeirdre A Harford, Kit Green Sanderson, Kirk A J Stephenson, et al.
Human Molecular Genetics|April 24, 2025
Defective IFT57 underlies a novel cause of Bardet-Biedl syndromeAlexandra Nitoiu, Qihong Zhang, Erika Tavares, et al.
NPJ Genomic Medicine|March 28, 2026
A novel phenotype-guided genome analysis pipeline for variant discoveryLayla Ahmed, Erika Tavares, Janice Min Li, et al.
Investigative Ophthalmology & Visual Science|September 4, 2020
Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant ExonizationMatteo Di Scipio, Erika Tavares, Shriya Deshmukh, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Aesthetic Surgery Journal|June 30, 2019
A Simple Clinical Application for Locating the Frontotemporal Branch of the Facial Nerve Using the Zygomatic Arch and the TragusKit Green Sanderson, Alyssa Conti, Mariah Colussi, et al.
BMJ Case Reports|November 2, 2021
Pigmentary retinopathy masked by asymmetric acquired phenomenaKit Green Sanderson, Kirk A J Stephenson, Adrian Dockery, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 23, 2020
Rod bipolar cell dysfunction in POLG retinopathyKit Green Sanderson, Eoghan Millar, Anupreet Tumber, et al.
BMJ Case Reports|February 10, 2021
Monocular syphilitic uveitisDeirdre A Harford, Kit Green Sanderson, Kirk A J Stephenson, et al.
Human Molecular Genetics|April 24, 2025
Defective IFT57 underlies a novel cause of Bardet-Biedl syndromeAlexandra Nitoiu, Qihong Zhang, Erika Tavares, et al.
NPJ Genomic Medicine|March 28, 2026
A novel phenotype-guided genome analysis pipeline for variant discoveryLayla Ahmed, Erika Tavares, Janice Min Li, et al.
Investigative Ophthalmology & Visual Science|September 4, 2020
Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant ExonizationMatteo Di Scipio, Erika Tavares, Shriya Deshmukh, et al.
Pageof 1