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Detecting inversions in routine molecular diagnosis in MMR genes.
Kasper, Edwige; Coutant, Sophie; Manase, Sandrine; Vasseur, Stéphanie; Macquère, Pierre; Bougeard, Gaëlle; Faivre, Laurence; Ingster, Olivier; Baert-Desurmont, Stéphanie; Houdayer, Claude.
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  • Kasper E; Department of Genetics, Normandy Center for Genomic and Personalized Medicine, UNIROUEN, Inserm U1245 and Rouen University Hospital, CHU Rouen, Normandie University, 76000, Rouen, France. edwige.kasper@chu-rouen.fr.
  • Coutant S; Department of Genetics, Normandy Center for Genomic and Personalized Medicine, UNIROUEN, Inserm U1245 and Rouen University Hospital, CHU Rouen, Normandie University, 76000, Rouen, France.
  • Manase S; Department of Genetics, Normandy Center for Genomic and Personalized Medicine, UNIROUEN, Inserm U1245 and Rouen University Hospital, CHU Rouen, Normandie University, 76000, Rouen, France.
  • Vasseur S; Department of Genetics, Normandy Center for Genomic and Personalized Medicine, UNIROUEN, Inserm U1245 and Rouen University Hospital, CHU Rouen, Normandie University, 76000, Rouen, France.
  • Macquère P; Department of Genetics, Normandy Center for Genomic and Personalized Medicine, UNIROUEN, Inserm U1245 and Rouen University Hospital, CHU Rouen, Normandie University, 76000, Rouen, France.
  • Bougeard G; Department of Genetics, Normandy Center for Genomic and Personalized Medicine, UNIROUEN, Inserm U1245 and Rouen University Hospital, CHU Rouen, Normandie University, 76000, Rouen, France.
  • Faivre L; Centre de Référence Maladies Rares, «Anomalies du Développement ET Syndromes Malformatifs¼, Centre de Génétique, FHU-TRANSLAD et Institut GIMI, 77908, Dijon, France.
  • Ingster O; UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, 77908, Dijon, France.
  • Baert-Desurmont S; Department of Genetics, University Hospital Centre Angers, Angers, Pays de la Loire, France.
  • Houdayer C; Department of Genetics, Normandy Center for Genomic and Personalized Medicine, UNIROUEN, Inserm U1245 and Rouen University Hospital, CHU Rouen, Normandie University, 76000, Rouen, France.
Fam Cancer ; 21(4): 423-428, 2022 10.
Article en En | MEDLINE | ID: mdl-34997397
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Neoplasias Colorrectales / Neoplasias Colorrectales Hereditarias sin Poliposis / Neoplasias del Colon Tipo de estudio: Diagnostic_studies Idioma: En Revista: Fam Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Neoplasias Colorrectales / Neoplasias Colorrectales Hereditarias sin Poliposis / Neoplasias del Colon Tipo de estudio: Diagnostic_studies Idioma: En Revista: Fam Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article