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P M Cremers

Showing results (11-20 of 307) with videos related to

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Novartis Foundation Symposium|January 31, 2004
The expanding roles of ABCA4 and CRB1 in inherited blindnessF P M Cremers, A Maugeri, A I den Hollander, et al.
Progress in Retinal and Eye Research|July 18, 2008
Leber congenital amaurosis: genes, proteins and disease mechanismsAnneke I den Hollander, Ronald Roepman, Robert K Koenekoop, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 15, 2012
Identification and analysis of inherited retinal disease genesKornelia Neveling, Anneke I den Hollander, Frans P M Cremers, et al.
International Journal of Molecular Sciences|April 3, 2021
The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing LossSuzanne E de Bruijn, Zeinab Fadaie, Frans P M Cremers, et al.
Human Molecular Genetics|August 9, 2023
Stargardt disease-associated missense and synonymous ABCA4 variants result in aberrant splicingMelita Kaltak, Zelia Corradi, Rob W J Collin, et al.
Clinical & Experimental Ophthalmology|July 27, 2007
Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutionsRobert K Koenekoop, Irma Lopez, Anneke I den Hollander, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 13, 2002
[From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa]F P M Cremers, A Maugeri, B J Klevering, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Mutation- and tissue-specific alterations of RPGR transcriptsFabian Schmid, Esther Glaus, Frans P M Cremers, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 24, 2019
The absence of fundus abnormalities in Stargardt diseaseNathalie M Bax, Stanley Lambertus, Frans P M Cremers, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 23, 2004
The spectrum of retinal phenotypes caused by mutations in the ABCA4 geneB Jeroen Klevering, August F Deutman, Alessandra Maugeri, et al.
Pageof 31

Showing results (11-20 of 307) with videos related to

Sort By:
Pageof 31
Novartis Foundation Symposium|January 31, 2004
The expanding roles of ABCA4 and CRB1 in inherited blindnessF P M Cremers, A Maugeri, A I den Hollander, et al.
Progress in Retinal and Eye Research|July 18, 2008
Leber congenital amaurosis: genes, proteins and disease mechanismsAnneke I den Hollander, Ronald Roepman, Robert K Koenekoop, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 15, 2012
Identification and analysis of inherited retinal disease genesKornelia Neveling, Anneke I den Hollander, Frans P M Cremers, et al.
International Journal of Molecular Sciences|April 3, 2021
The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing LossSuzanne E de Bruijn, Zeinab Fadaie, Frans P M Cremers, et al.
Human Molecular Genetics|August 9, 2023
Stargardt disease-associated missense and synonymous ABCA4 variants result in aberrant splicingMelita Kaltak, Zelia Corradi, Rob W J Collin, et al.
Clinical & Experimental Ophthalmology|July 27, 2007
Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutionsRobert K Koenekoop, Irma Lopez, Anneke I den Hollander, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 13, 2002
[From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa]F P M Cremers, A Maugeri, B J Klevering, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Mutation- and tissue-specific alterations of RPGR transcriptsFabian Schmid, Esther Glaus, Frans P M Cremers, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 24, 2019
The absence of fundus abnormalities in Stargardt diseaseNathalie M Bax, Stanley Lambertus, Frans P M Cremers, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 23, 2004
The spectrum of retinal phenotypes caused by mutations in the ABCA4 geneB Jeroen Klevering, August F Deutman, Alessandra Maugeri, et al.
Pageof 31