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European Journal of Human Genetics : EJHG|June 14, 2020
Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndromeMarc Tischkowitz, Chrystelle Colas, Sjaak Pouwels, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|April 18, 2013
Perivascular epithelioid cell tumor: the first malignant case report in the pancreasNajat Mourra, Thierry Lazure, Chrystelle Colas, et al.
European Journal of Cancer (Oxford, England : 1990)|April 27, 2020
Direct-to-consumer misleading information on cancer risks calls for an urgent clarification of health genetic testing performed by commercial companiesAntoine de Pauw, Mathias Schwartz, Chrystelle Colas, et al.
Familial Cancer|April 28, 2012
French experts report on MUTYH-associated polyposis (MAP)Bruno Buecher, Catherine Bonaïti, Marie-Pierre Buisine, et al.
Breast (Edinburgh, Scotland)|March 2, 2019
"Decoding hereditary breast cancer" benefits and questions from multigene panel testingChrystelle Colas, Lisa Golmard, Antoine de Pauw, et al.
Familial Cancer|October 16, 2014
Desmoid tumour in familial adenomatous polyposis patients: responses to treatmentsThibault Desurmont, Jérémie H Lefèvre, Conor Shields, et al.
European Journal of Human Genetics : EJHG|July 18, 2020
Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspringErell Guillerm, Magali Svrcek, Armelle Bardier-Dupas, et al.
Advances in Cancer Research|March 21, 2012
Lynch or not Lynch? Is that always a question?Chrystelle Colas, Florence Coulet, Magali Svrcek, et al.
European Journal of Human Genetics : EJHG|January 29, 2026
Results of a multigene panel testing approach targeting patients with suspected genetic predisposition to pancreatic ductal adenocarcinomaBruno Buecher, Mathilde Warcoin, Emilie Rolland, et al.
Bulletin Du Cancer|December 16, 2018
[Constitutional MMR deficiency: Genetic bases and clinical implications]Bruno Buecher, Marine Le Mentec, François Doz, et al.
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