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Author/Creator Auber, Bernd

11. Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer. Issue 7 (29th February 2016)

Authors:
Kast, Karin; Rhiem, Kerstin; Wappenschmidt, Barbara; Hahnen, Eric; Hauke, Jan; Bluemcke, Britta; Zarghooni, Verena; Herold, Natalie; Ditsch, Nina; Kiechle, Marion; Braun, Michael; Fischer, Christine; Dikow, Nicola; Schott, Sarah; Rahner, Nils; Niederacher, Dieter; Fehm, Tanja; Gehrig, Andrea; Mue...
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 7(2016)
Page Start:
465
Record Type:
Journal Article
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13. The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants. Issue 11 (11th January 2019)

Authors:
Schubert, Stephanie; van Luttikhuizen, Jana L.; Auber, Bernd; Schmidt, Gunnar; Hofmann, Winfried; Penkert, Judith; Davenport, Colin F.; Hille‐Betz, Ursula; Wendeburg, Lena; Bublitz, Janin; Tauscher, Marcel; Hackmann, Karl; Schröck, Evelin; Scholz, Caroline; Wallaschek, Hannah; Schlegelberger, Bri...
Journal:
International journal of cancer
Issue:
Volume 144:Issue 11(2019)
Page Start:
2683
Record Type:
Journal Article
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14. Two cancer‐predisposing variants in one family: Incidental finding of a fumarate hydrogenase (FH) germline variant in a family with Li–Fraumeni syndrome. Issue 10 (12th June 2018)

Authors:
Pahl, Lisa; Beier, Rita; von Neuhoff, Nils; Auber, Bernd; Höfs, Michaela; Prott, Eva‐Christina; Schlegelberger, Brigitte; Reinhardt, Dirk; Steinemann, Doris
Journal:
Pediatric blood & cancer
Issue:
Volume 65:Issue 10(2018)
Page Start:
n/a
Record Type:
Journal Article
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