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The Journal of Clinical Endocrinology and Metabolism|November 28, 2020
Screening of a Large Cohort of Asymptomatic SDHx Mutation Carriers in Routine PracticeClotilde Saie, Alexandre Buffet, Juliette Abeillon, et al.
Genes, Chromosomes & Cancer|January 25, 2023
A novel VCP::TFE3 gene fusion resulting from t(X;9)(p11.23;p13.3) chromosome translocation in TFE3 rearranged renal cancer cell carcinomaMarie Auvray Kuentz, Hélène Blons, Anne Paule Gimenez-Roqueplo, et al.
Plos One|May 9, 2012
Identity by descent mapping of founder mutations in cancer using high-resolution tumor SNP dataEric Letouzé, Aliou Sow, Fabien Petel, et al.
Cancer Cell|May 28, 2013
SDH mutations establish a hypermethylator phenotype in paragangliomaEric Letouzé, Cosimo Martinelli, Céline Loriot, et al.
Plos One|September 19, 2009
The Warburg effect is genetically determined in inherited pheochromocytomasJudith Favier, Jean-Jacques Brière, Nelly Burnichon, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Juvenile hemochromatosis HJV-related revealed by cardiogenic shockMounir Filali, Claire Le Jeunne, Eric Durand, et al.
European Journal of Human Genetics : EJHG|August 2, 2022
Minors at risk of von Hippel-Lindau disease: 10 years' experience of predictive genetic testing and follow-up adherenceRoseline Vibert, Khadija Lahlou-Laforêt, Maryam Samadi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 11, 2018
Telomerase Activation and ATRX Mutations Are Independent Risk Factors for Metastatic Pheochromocytoma and ParagangliomaSylvie Job, Irena Draskovic, Nelly Burnichon, et al.
Journal of Medical Genetics|March 17, 2019
Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paragangliomaLaurène Ben Aim, Pascal Pigny, Luis Jaime Castro-Vega, et al.
Clinical Endocrinology|November 9, 2021
Genetic spectrum in a Canadian cohort of apparently sporadic pheochromocytomas and paragangliomas: New data on multigene panel retesting over timeStéfanie Parisien-La Salle, Nadine Dumas, Karine Bédard, et al.
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