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Edwin M Stone

Showing results (341-350 of 384) with videos related to

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Human Molecular Genetics|April 30, 2002
VSX1: a gene for posterior polymorphous dystrophy and keratoconusElise Héon, Alex Greenberg, Kelly K Kopp, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 13, 2007
Human cone photoreceptor dependence on RPE65 isomeraseSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
European Journal of Human Genetics : EJHG|November 16, 2006
Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10Dominic R A White, Anuradha Ganesh, Darryl Nishimura, et al.
Experimental Eye Research|May 17, 2002
Macular pigment and lutein supplementation in choroideremiaJacque L Duncan, Tomas S Aleman, Leigh M Gardner, et al.
Investigative Ophthalmology & Visual Science|February 19, 2008
Retinal disease in Usher syndrome III caused by mutations in the clarin-1 geneWaldo Herrera, Tomas S Aleman, Artur V Cideciyan, et al.
Human Molecular Genetics|March 31, 2011
Copy number variations on chromosome 12q14 in patients with normal tension glaucomaJohn H Fingert, Alan L Robin, Jennifer L Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 12, 2011
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndromeEdwin M Stone, Artur V Cideciyan, Tomas S Aleman, et al.
Human Mutation|October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone SyndromeAlan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Investigative Ophthalmology & Visual Science|February 28, 2007
Macular pigment and lutein supplementation in ABCA4-associated retinal degenerationsTomas S Aleman, Artur V Cideciyan, Elizabeth A M Windsor, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
Pageof 39

Showing results (341-350 of 384) with videos related to

Sort By:
Pageof 39
Human Molecular Genetics|April 30, 2002
VSX1: a gene for posterior polymorphous dystrophy and keratoconusElise Héon, Alex Greenberg, Kelly K Kopp, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 13, 2007
Human cone photoreceptor dependence on RPE65 isomeraseSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
European Journal of Human Genetics : EJHG|November 16, 2006
Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10Dominic R A White, Anuradha Ganesh, Darryl Nishimura, et al.
Experimental Eye Research|May 17, 2002
Macular pigment and lutein supplementation in choroideremiaJacque L Duncan, Tomas S Aleman, Leigh M Gardner, et al.
Investigative Ophthalmology & Visual Science|February 19, 2008
Retinal disease in Usher syndrome III caused by mutations in the clarin-1 geneWaldo Herrera, Tomas S Aleman, Artur V Cideciyan, et al.
Human Molecular Genetics|March 31, 2011
Copy number variations on chromosome 12q14 in patients with normal tension glaucomaJohn H Fingert, Alan L Robin, Jennifer L Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 12, 2011
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndromeEdwin M Stone, Artur V Cideciyan, Tomas S Aleman, et al.
Human Mutation|October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone SyndromeAlan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Investigative Ophthalmology & Visual Science|February 28, 2007
Macular pigment and lutein supplementation in ABCA4-associated retinal degenerationsTomas S Aleman, Artur V Cideciyan, Elizabeth A M Windsor, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
Pageof 39