The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: high frequency of FANCM pathogenic variants

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Source: International Journal of Cancer - November 13, 2018 Category: Cancer & Oncology Authors: Stephanie Schubert, Jana L. Luttikhuizen, Bernd Auber, Gunnar Schmidt, Winfried Hofmann, Judith Penkert, Colin F. Davenport, Ursula Hille ‐Betz, Lena Wendeburg, Janin Bublitz, Marcel Tauscher, Karl Hackmann, Evelin Schroeck, Caroline Scholz Tags: Research Article Source Type: research