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American Journal of Human Genetics|June 3, 2017
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVREvangelia S Panagiotou, Carla Sanjurjo Soriano, James A Poulter, et al.
Ophthalmology|March 19, 2013
Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunctionSusanne Roosing, L Ingeborgh van den Born, Carel B Hoyng, et al.
American Journal of Human Genetics|February 18, 2010
Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathyKonstantinos Nikopoulos, Christian Gilissen, Alexander Hoischen, et al.
American Journal of Human Genetics|August 13, 2011
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosaRıza Köksal Ozgül, Anna M Siemiatkowska, Didem Yücel, et al.
Cancer|January 3, 2025
Comorbid conditions and survival among Black women with ovarian cancerAlicia R Richards, Courtney E Johnson, Nachalie Ramos Montalvo, et al.
JAMA|July 17, 2024
Endometriosis Typology and Ovarian Cancer RiskMollie E Barnard, Leslie V Farland, Bin Yan, et al.
British Journal of Cancer|August 3, 2023
Association of inflammation-related exposures and ovarian cancer survival in a multi-site cohort study of Black womenCourtney E Johnson, Anthony J Alberg, Elisa V Bandera, et al.
Investigative Ophthalmology & Visual Science|February 5, 2010
A novel nonsense mutation in CEP290 induces exon skipping and leads to a relatively mild retinal phenotypeKarin W Littink, Jan-Willem R Pott, Rob W J Collin, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 15, 2020
Metabolic Pathway Analysis and Effectiveness of Tamoxifen in Danish Breast Cancer PatientsThomas P Ahern, Lindsay J Collin, James W Baurley, et al.
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