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Characterization of rare germline variants in familial multiple myeloma
C. Catalano, N. Paramasivam, J. Blocka, S. Giangiobbe, S. Huhn, M. Schlesner, N. Weinhold, R. Sijmons, M. de Jong, C. Langer, KD. Preuss, B. Nilsson, B. Durie, H. Goldschmidt, OR. Bandapalli, K. Hemminki, A. Försti
Language English Country United States
Document type Letter, Research Support, Non-U.S. Gov't
Grant support
11R/2019
José Carreras Leukämie-Stiftung (Deutsche José Carreras Leukämie-Stiftung)
NLK
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- MeSH
- Genetic Predisposition to Disease MeSH
- Humans MeSH
- Mutation, Missense MeSH
- Multiple Myeloma genetics MeSH
- Pedigree MeSH
- Germ-Line Mutation * MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Letter MeSH
- Research Support, Non-U.S. Gov't MeSH
Bioinformatics and Omics Data Analytics German Cancer Research Center Heidelberg Germany
Cedars Sinai Cancer Center Los Angeles CA USA
Department of Internal Medicine 5 University of Heidelberg Heidelberg Germany
Division of Cancer Epidemiology German Cancer Research Center Heidelberg Germany
Division of Molecular Genetic Epidemiology German Cancer Research Center Heidelberg Germany
Division of Pediatric Neurooncology German Cancer Research Center Heidelberg Germany
Faculty of Medicine and Biomedical Center in Pilsen Charles University Prague Pilsen Czech Republic
Hematology and Transfusion Medicine Department of Laboratory Medicine Lund University Lund Sweden
Hopp Children's Cancer Center Heidelberg Germany
Kempten Clinic Kempten Germany
National Center for Tumor Diseases Heidelberg Heidelberg Germany
University Medical Center Groningen University of Groningen Groningen The Netherlands
References provided by Crossref.org
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