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J Collin

Showing results (391-400 of 449) with videos related to

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Molecular Genetics & Genomic Medicine|January 29, 2015
Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophyGaluh D N Astuti, Vincent Sun, Miriam Bauwens, et al.
Clinical Genetics|November 9, 2012
Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from PakistanM I Khan, M Ajmal, S Micheal, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 4, 2025
Homologous recombination deficiency and survival in ovarian high-grade serous carcinoma by self-reported raceKatherine A Lawson-Michod, Courtney E Johnson, Mollie E Barnard, et al.
American Journal of Human Genetics|March 10, 2009
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosaHui Wang, Anneke I den Hollander, Yalda Moayedi, et al.
Investigative Ophthalmology & Visual Science|November 18, 2015
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis PigmentosaKristof Van Schil, B Jeroen Klevering, Bart P Leroy, et al.
Cancer Medicine|October 24, 2024
Tattoos and Risk of Hematologic Cancer: A Population-Based Case-Control Study in UtahRachel D McCarty, Britton Trabert, David Kriebel, et al.
Ophthalmology|January 19, 2010
Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophyAlberta A H J Thiadens, Susanne Roosing, Rob W J Collin, et al.
American Journal of Obstetrics and Gynecology|April 28, 2023
Role of neighborhood context in ovarian cancer survival disparities: current research and future directionsScarlett L Gomez, Ekaterina Chirikova, Valerie McGuire, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 12, 2011
Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosaMaleeha Azam, Rob W J Collin, Ayesha Malik, et al.
Acta Ophthalmologica|November 12, 2014
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular featuresRamon A C van Huet, Anna M Siemiatkowska, Riza K Özgül, et al.
Pageof 45

Showing results (391-400 of 449) with videos related to

Sort By:
Pageof 45
Molecular Genetics & Genomic Medicine|January 29, 2015
Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophyGaluh D N Astuti, Vincent Sun, Miriam Bauwens, et al.
Clinical Genetics|November 9, 2012
Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from PakistanM I Khan, M Ajmal, S Micheal, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 4, 2025
Homologous recombination deficiency and survival in ovarian high-grade serous carcinoma by self-reported raceKatherine A Lawson-Michod, Courtney E Johnson, Mollie E Barnard, et al.
American Journal of Human Genetics|March 10, 2009
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosaHui Wang, Anneke I den Hollander, Yalda Moayedi, et al.
Investigative Ophthalmology & Visual Science|November 18, 2015
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis PigmentosaKristof Van Schil, B Jeroen Klevering, Bart P Leroy, et al.
Cancer Medicine|October 24, 2024
Tattoos and Risk of Hematologic Cancer: A Population-Based Case-Control Study in UtahRachel D McCarty, Britton Trabert, David Kriebel, et al.
Ophthalmology|January 19, 2010
Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophyAlberta A H J Thiadens, Susanne Roosing, Rob W J Collin, et al.
American Journal of Obstetrics and Gynecology|April 28, 2023
Role of neighborhood context in ovarian cancer survival disparities: current research and future directionsScarlett L Gomez, Ekaterina Chirikova, Valerie McGuire, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 12, 2011
Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosaMaleeha Azam, Rob W J Collin, Ayesha Malik, et al.
Acta Ophthalmologica|November 12, 2014
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular featuresRamon A C van Huet, Anna M Siemiatkowska, Riza K Özgül, et al.
Pageof 45