Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia‐like phenotype, and no chromosome fragility

Author:

Keupp Katharina1,Hampp Stephanie2,Hübbel Annette1,Maringa Monika1,Kostezka Sarah2,Rhiem Kerstin1,Waha Anke1,Wappenschmidt Barbara1,Pujol Roser345,Surrallés Jordi345,Schmutzler Rita K.1,Wiesmüller Lisa2,Hahnen Eric1ORCID

Affiliation:

1. Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany University Hospital of Cologne Cologne Germany

2. Department of Obstetrics and Gynecology Ulm University Ulm Germany

3. Department of Genetics and Biomedical Research Institute Hospital de Sant Pau Barcelona Spain

4. Department of Genetics and Microbiology Universitat Autònoma de Barcelona Barcelona Spain

5. Center for Biomedical Network Research on Rare Diseases Barcelona Spain

Funder

Ministerio de Economía y Competitividad

Deutsche Krebshilfe

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

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