Items where Author is "Faust, U."

Conference or Workshop Item

Habhab, W. and Faust, U. and Guenther, G. and Siebers-Renelt, U. and Kiechle, M. and Ott, C. and Dikow, N. and Kast, K. and Vesper, A. and Solbach, C. and Harbeck, N. and Stiller, M. and Gehrig, A. and Thomssen, C. and Wallaschek, H. and Arnold, N. and Holzhauser, I. and Kaulfuss, S. and Volk, A. and Janni, W. and Engel, C. and Schmutzler, R. and Riess, O. and Schroeder, C. and Bosse, K. (2020) Clinical and molecular characterization of 1253 carriers of a deleterious CHEK2 mutation from the German Consortium for Hereditary Breast and Ovarian Cancer (GC-HBOC). In: 53rd European Society of Human Genetics (ESHG) Conference, June 6–9, 2020, Virtuell.

Bosse, K. and Faust, U. and Gruber, I. and Habhab, W. and Guenther, G. and Siebers-Renelt, U. and Kiechle, M. and Speiser, D. and Dikow, N. and Kast, K. and Arnold, N. and Vesper, A.-S. and Harbeck, N. and Briest, S. and Thomssen, C. and Gehrig, A. and Wallaschek, H. and Solbach, C. and Wolf, M. and Witzel, I. and Holzhauser, I. and Kaulfuss, S. and Janni, W. and Engel, C. and Riess, O. and Schmutzler, R. and Schroeder, C. (2020) Clinical-pathological Characterization of 1078 Advice Seekers with pathogenic CHEK2 Mutation from the German Consortium of Familial Breast and Ovarian Cancer (DK-FBREK). In: 40. Jahrestagung der Deutschen Gesellschaft für Senologie e.V., 25.-27.06.2020, Congress Center München.