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2019
Hueneburg, Robert, Aretz, Stefan 
ORCID: 0000-0002-5228-1890, Buettner, Reinhard, Daum, Severin, Engel, Christoph ORCID: 0000-0002-7247-282X, Fechner, Guido, Habermann, Jens K., Heling, Dominik, Hoffmann, Katrin, Holinski-Feder, Elke, Kloor, Matthias, von Knebel-Doeberitz, Magnus, Loeffler, Markus, Moeslein, Gabriela, Perne, Claudia, Redler, Silke, Riess, Olaf, Schmiegel, Wolff, Seufferlein, Thomas, Siebers-Renelt, Ulrike, Steinke-Lange, Verena, Tecklenburg, Johanna, Vangala, Deepak, Vilz, Tim, Weitz, Juergen, Wiedenmann, Bertram, Strassburg, Christian P. and Nattermann, Jacob
(2019).
Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients.
Z. Gastroent., 57 (11).
S. 1309 - 1321.
STUTTGART:
GEORG THIEME VERLAG KG.
ISSN 1439-7803
2018
Kayser, Katrin, Degenhardt, Franziska, Holzapfel, Stefanie, Horpaopan, Sukanya, Peters, Sophia, Spier, Isabel, Morak, Monika, Vangala, Deepak, Rahner, Nils, von Knebel-Doeberitz, Magnus, Schackert, Hans K., Engel, Christoph ORCID: 0000-0002-7247-282X, Buettner, Reinhard, Wijnen, Juul, Doerks, Tobias, Bork, Peer, Moebus, Susanne, Herms, Stefan ORCID: 0000-0002-2786-8200, Fischer, Sascha, Hoffmann, Per, Aretz, Stefan ORCID: 0000-0002-5228-1890 and Steinke-Lange, Verena
(2018).
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.
Int. J. Cancer, 143 (11).
S. 2800 - 2814.
HOBOKEN:
WILEY.
ISSN 1097-0215
2014
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