The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants-Reference-Cited by-同舟云学术

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

Published:2019-01-11 Issue:11 Volume:144 Page:2683-2694
ISSN:0020-7136
Container-title:International Journal of Cancer
language:en
Short-container-title:Int. J. Cancer

Author:

Schubert Stephanie¹,Luttikhuizen Jana L.¹,Auber Bernd¹,Schmidt Gunnar¹,Hofmann Winfried¹,Penkert Judith¹,Davenport Colin F.²,Hille‐Betz Ursula³,Wendeburg Lena¹,Bublitz Janin¹,Tauscher Marcel¹,Hackmann Karl⁴⁵⁶⁷,Schröck Evelin⁴⁶⁷,Scholz Caroline¹,Wallaschek Hannah¹,Schlegelberger Brigitte¹,Illig Thomas¹,Steinemann Doris¹^ORCID

Affiliation:

1. Department of Human GeneticsHannover Medical School Hannover Germany

2. Research Core Unit GenomicsHannover Medical School Hannover Germany

3. Department of Obstetrics and GynaecologyHannover Medical School Hannover Germany

4. Institute for Clinical Genetics, Faculty of Medicine Carl Gustav Carus, TU Dresden Dresden Germany

5. German Cancer Consortium (DKTK) Dresden Germany

6. German Cancer Research Center (DKFZ) Heidelberg Germany

7. National Center for Tumor Diseases (NCT) Partner Site Dresden Dresden Germany

Funder

The Claudia-von-Schilling foundation Hannover, Germany

MD/PhD program molecular medicine, The Hannover Biomedical Research School

Publisher