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Number of items: 4.

Journal Article

Binder, Hans, Hopp, Lydia, Schweiger, Michal R., Hoffmann, Steve, Juehling, Frank, Kerick, Martin ORCID: 0000-0002-6298-4514, Timmermann, Bernd, Siebert, Susann, Grimm, Christina ORCID: 0000-0002-4676-8870, Nersisyan, Lilit ORCID: 0000-0001-8525-420X, Arakelyan, Arsen ORCID: 0000-0002-6851-1056, Herberg, Maria, Buske, Peter, Loeffler-Wirth, Henry, Rosolowski, Maciej, Engel, Christoph ORCID: 0000-0002-7247-282X, Przybilla, Jens, Peifer, Martin ORCID: 0000-0002-5243-5503, Friedrichs, Nicolaus, Moeslein, Gabriela, Odenthal, Margarete, Hussong, Michelle, Peters, Sophia, Holzapfel, Stefanie, Nattermann, Jacob, Hueneburg, Robert, Schmiegel, Wolff, Royer-Pokora, Brigitte, Aretz, Stefan ORCID: 0000-0002-5228-1890, Kloth, Michael, Kloor, Matthias, Buettner, Reinhard, Galle, Joerg and Loeffler, Markus (2017). Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome. J. Pathol., 243 (2). S. 242 - 255. HOBOKEN: WILEY. ISSN 1096-9896

Rahner, Nils, Nuernberg, Gudrun, Finis, David, Nuernberg, Peter and Royer-Pokora, Brigitte (2016). A novel C8orf37 splice mutation and genotype-phenotype correlation for cone-rod dystrophy. Ophthalmic Genet., 37 (3). S. 294 - 301. PHILADELPHIA: TAYLOR & FRANCIS INC. ISSN 1744-5094

Steinke, Verena, Holzapfel, Stefanie, Loeffler, Markus, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K., Goergens, Heike, Pox, Christian, Royer-Pokora, Brigitte, von Knebel-Doeberitz, Magnus, Buettner, Reinhard, Propping, Peter and Engel, Christoph ORCID: 0000-0002-7247-282X (2014). Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families. Int. J. Cancer, 135 (1). S. 69 - 78. HOBOKEN: WILEY. ISSN 1097-0215

Yang, Rongxi, Chen, Bowang, Pfuetze, Katrin, Buch, Stephan, Steinke, Verena, Holinski-Feder, Elke, Stoecker, Sarah, von schoenfels, Witigo, Becker, Thomas, Schackert, Hans K., Royer-Pokora, Brigitte, Kloor, Matthias, Schmiegel, Wolff H., Buettner, Reinhard, Engel, Christoph ORCID: 0000-0002-7247-282X, Puertolas, Jesus Lascorz, Foersti, Asta, Kunkel, Nelli, Bugert, Peter, Schreiber, Stefan, Krawczak, Michael ORCID: 0000-0003-2603-1502, Schafmayer, Clemens, Propping, Peter, Hampe, Jochen ORCID: 0000-0002-2421-6127, Hemminki, Kari and Burwinkel, Barbara (2014). Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3. Carcinogenesis, 35 (2). S. 315 - 324. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2180

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