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Alex V Levin

Ophthalmic genetics

Showing results (1-10 of 15) with videos related to

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Ophthalmic Genetics|February 16, 2019
Ophthalmologic findings in the Cornelia de Lange syndromeAngell Shi, Alex V Levin
Ophthalmic Genetics|April 11, 2012
Ocular anomalies in an infant with Klinefelter SyndromeAlexander T Juhn, Naeem U Nabi, Alex V Levin
Ophthalmic Genetics|February 20, 2016
Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK geneYu-Hung Lai, Jenina E Capasso, Richard Kaiser, et al.
Ophthalmic Genetics|December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosaDiego I Paredes, Nicholas R Bello, Jenina E Capasso, et al.
Ophthalmic Genetics|October 8, 2013
Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and SonKarthikeyan Arcot Sadagopan, Robert Battista, Rosanne B Keep, et al.
Ophthalmic Genetics|April 25, 2007
Psychosocial adjustment to visual loss in patients with retinitis pigmentosaDalbhir Jangra, Anuradha Ganesh, Robin Thackray, et al.
Ophthalmic Genetics|March 18, 2006
The ocular manifestations of Jacobsen syndrome: a report of four cases and a review of the literatureGarfield L Miller, Sohel Somani, Malgorzata J M Nowaczyk, et al.
Ophthalmic Genetics|April 21, 2018
Ophthalmic manifestations of Heimler syndrome due to PEX6 mutationsNutsuchar Wangtiraumnuay, Waleed Abed Alnabi, Mai Tsukikawa, et al.
Ophthalmic Genetics|April 25, 2007
Attitudes regarding predictive testing for retinitis pigmentosaEedy Mezer, Riyana Babul-Hirji, Richard Wise, et al.
Ophthalmic Genetics|January 24, 2017
Spectral-domain optical coherence tomography findings in Alström syndromeGad Dotan, Vikas Khetan, Jan D Marshall, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Ophthalmic Genetics|February 16, 2019
Ophthalmologic findings in the Cornelia de Lange syndromeAngell Shi, Alex V Levin
Ophthalmic Genetics|April 11, 2012
Ocular anomalies in an infant with Klinefelter SyndromeAlexander T Juhn, Naeem U Nabi, Alex V Levin
Ophthalmic Genetics|February 20, 2016
Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK geneYu-Hung Lai, Jenina E Capasso, Richard Kaiser, et al.
Ophthalmic Genetics|December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosaDiego I Paredes, Nicholas R Bello, Jenina E Capasso, et al.
Ophthalmic Genetics|October 8, 2013
Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and SonKarthikeyan Arcot Sadagopan, Robert Battista, Rosanne B Keep, et al.
Ophthalmic Genetics|April 25, 2007
Psychosocial adjustment to visual loss in patients with retinitis pigmentosaDalbhir Jangra, Anuradha Ganesh, Robin Thackray, et al.
Ophthalmic Genetics|March 18, 2006
The ocular manifestations of Jacobsen syndrome: a report of four cases and a review of the literatureGarfield L Miller, Sohel Somani, Malgorzata J M Nowaczyk, et al.
Ophthalmic Genetics|April 21, 2018
Ophthalmic manifestations of Heimler syndrome due to PEX6 mutationsNutsuchar Wangtiraumnuay, Waleed Abed Alnabi, Mai Tsukikawa, et al.
Ophthalmic Genetics|April 25, 2007
Attitudes regarding predictive testing for retinitis pigmentosaEedy Mezer, Riyana Babul-Hirji, Richard Wise, et al.
Ophthalmic Genetics|January 24, 2017
Spectral-domain optical coherence tomography findings in Alström syndromeGad Dotan, Vikas Khetan, Jan D Marshall, et al.
Pageof 2