Universität zu Köln

Journal Article

Gallon, Richard ORCID: 0000-0002-5395-0099, Muehlegger, Barbara, Wenzel, Soeren-Sebastian, Sheth, Harsh, Hayes, Christine, Aretz, Stefan ORCID: 0000-0002-5228-1890, Dahan, Karin, Foulkes, William, Kratz, Christian P., Ripperger, Tim, Azizi, Amedeo A., Feldman, Hagit Baris, Chong, Anne-Laure, Demirsoy, Ugur, Florkin, Benoit, Imschweiler, Thomas, Januszkiewicz-Lewandowska, Danuta ORCID: 0000-0003-2332-2750, Lobitz, Stephan ORCID: 0000-0001-5398-0610, Nathrath, Michaela, Pander, Hans-Juergen, Perez-Alonso, Vanesa, Perne, Claudia, Ragab, Iman, Rosenbaum, Thorsten, Rueda, Daniel ORCID: 0000-0002-5377-8890, Seidel, Markus G. ORCID: 0000-0003-0981-8661, Suerink, Manon, Taeubner, Julia, Zimmermann, Stefanie-Yvonne, Zschocke, Johannes, Borthwick, Gillian M., Burn, John, Jackson, Michael S., Santibanez-Koref, Mauro and Wimmer, Katharina (2019). A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes. Hum. Mutat., 40 (5). S. 649 - 656. HOBOKEN: WILEY. ISSN 1098-1004

Gonzalez-Acosta, Maribel ORCID: 0000-0002-2468-3876, Marin, Fatima ORCID: 0000-0003-3534-0091, Puliafito, Benjamin, Bonifaci, Nuria, Fernandez, Anna, Navarro, Matilde, Salvador, Hector ORCID: 0000-0002-2515-0019, Balaguer, Francesc, Iglesias, Silvia, Velasco, Angela, Garces, Elia Grau, Moreno, Victor ORCID: 0000-0002-2818-5487, Gonzalez-Granado, Luis Ignacio ORCID: 0000-0001-6917-8980, Guerra-Garcia, Pilar ORCID: 0000-0002-7740-0614, Ayala, Rosa, Florkin, Benoit, Kratz, Christian, Ripperger, Tim, Rosenbaum, Thorsten, Januszkiewicz-Lewandowska, Danuta, Azizi, Amedeo A., Ragab, Iman, Nathrath, Michaela, Pander, Hans-Juergen, Lobitz, Stephan, Suerink, Manon, Dahan, Karin, Imschweiler, Thomas, Demirsoy, Ugur, Brunet, Joan ORCID: 0000-0003-1945-3512, Lazaro, Conxi, Rueda, Daniel ORCID: 0000-0002-5377-8890, Wimmer, Katharina, Capella, Gabriel and Pineda, Marta (2020). High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers. J. Med. Genet., 57 (4). S. 269 - 274. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-6244