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Jenina E Capasso

Showing results (1-10 of 22) with videos related to

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Current Opinion in Ophthalmology|July 11, 2014
The cost of genetic testing for ocular disease: who pays?Jenina E Capasso
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.
American Journal of Medical Genetics. Part A|September 5, 2018
Ocular manifestations of Emanuel syndromeBrooke D Saffren, Jenina E Capasso, Mario Zanolli, et al.
Current Opinion in Ophthalmology|July 30, 2013
Lyonization in ophthalmologyWadakarn Wuthisiri, Michelle D Lingao, Jenina E Capasso, et al.
Taiwan Journal of Ophthalmology|January 22, 2024
Genetics of the anterior segment dysgenesisDiego I Paredes, Jenina E Capasso, Celeste S Wyman, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Early onset ectopia lentis due to a FBN1 mutation with non-penetranceLi Zhang, Yu-Hung Lai, Jenina E Capasso, 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.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 19, 2018
Ocular manifestations of PACS1 mutationMaria Pefkianaki, Adele Schneider, Jenina E Capasso, et al.
Retinal Cases & Brief Reports|October 30, 2023
TWO CASES OF CRB1-RELATED RETINAL DYSTROPHY ASSOCIATED WITH RETINAL MASSESNicholas R Bello, Phattrawan Pisuchpen, Thales A C de Guimarães, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Current Opinion in Ophthalmology|July 11, 2014
The cost of genetic testing for ocular disease: who pays?Jenina E Capasso
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.
American Journal of Medical Genetics. Part A|September 5, 2018
Ocular manifestations of Emanuel syndromeBrooke D Saffren, Jenina E Capasso, Mario Zanolli, et al.
Current Opinion in Ophthalmology|July 30, 2013
Lyonization in ophthalmologyWadakarn Wuthisiri, Michelle D Lingao, Jenina E Capasso, et al.
Taiwan Journal of Ophthalmology|January 22, 2024
Genetics of the anterior segment dysgenesisDiego I Paredes, Jenina E Capasso, Celeste S Wyman, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Early onset ectopia lentis due to a FBN1 mutation with non-penetranceLi Zhang, Yu-Hung Lai, Jenina E Capasso, 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.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 19, 2018
Ocular manifestations of PACS1 mutationMaria Pefkianaki, Adele Schneider, Jenina E Capasso, et al.
Retinal Cases & Brief Reports|October 30, 2023
TWO CASES OF CRB1-RELATED RETINAL DYSTROPHY ASSOCIATED WITH RETINAL MASSESNicholas R Bello, Phattrawan Pisuchpen, Thales A C de Guimarães, et al.
Pageof 3