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Gynecologic Oncology|March 12, 2026
Peritoneal cancer risk after risk reducing salpingo-oophorectomy, impact of mutational status and STIC lesionsClaire Saule, Enora Laas, Nina Weber, et al.
Journal of Medical Genetics|April 17, 2014
Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD)Katharina Wimmer, Christian P Kratz, Hans F A Vasen, et al.
Bulletin Du Cancer|January 31, 2008
[Clinical and molecular consequences of microsatellite instability in human cancers]Richard Hamelin, Alexandra Chalastanis, Chrystelle Colas, et al.
Familial Cancer|February 7, 2025
Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencingMorgane Boedec, Camille Aucouturier, Mathias Cavaillé, et al.
Journal of Medical Genetics|September 29, 2023
Neurofibromatosis type 1 mosaicism in patients with constitutional mismatch repair deficiencyLéa Guerrini-Rousseau, Eric Pasmant, Martine Muleris, et al.
Clinical Genetics|August 22, 2019
Familial pancreatic adenocarcinoma: A retrospective analysis of germline genetic testing in a French multicentre cohortMathias Schwartz, Clement Korenbaum, Meriem Benfoda, et al.
Journal of Medical Genetics|June 1, 2023
Adaptive nanopore sequencing to determine pathogenicity of BRCA1 exonic duplicationMathilde Filser, Mathias Schwartz, Kevin Merchadou, et al.
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