Hyperhaploid plasma cell myeloma characterized by poor outcome and monosomy 17 with frequently co-occurring TP53 mutations
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| Veröffentlicht in: | Blood cancer journal (New York) 2019-02, Vol.9 (3), p.20-20, Article 20 |
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| container_title | Blood cancer journal (New York) |
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| creator | Peterson, Jess F. Rowsey, Ross A. Marcou, Cherisse A. Pearce, Kathryn E. Williamson, Cynthia M. Frederick, Lori A. Greipp, Patricia T. Ketterling, Rhett P. Kumar, Shaji Viswanatha, David S. Polley, Mei-Yin Fink, James M. Reichard, Kaaren K. Van Dyke, Daniel L. Baughn, Linda B. |
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| doi_str_mv | 10.1038/s41408-019-0182-z |
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| subjects | 14/32 45/23 45/77 631/67/68 631/67/69 Adult Aged Aged, 80 and over Biomarkers, Tumor Biomedical and Life Sciences Biomedicine Cancer Research Chromosomes, Human, Pair 17 Correspondence Female Haploidy Hematology Humans In Situ Hybridization, Fluorescence Karyotype Male Middle Aged Monosomy Multiple Myeloma - diagnosis Multiple Myeloma - genetics Multiple Myeloma - mortality Mutation Oncology Prognosis Tumor Suppressor Protein p53 - genetics |
| title | Hyperhaploid plasma cell myeloma characterized by poor outcome and monosomy 17 with frequently co-occurring TP53 mutations |
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