Comprehensive genomic testing is required to assess for markers of poor prognosis in multiple myeloma
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference12 articles.
1. WHO: Classification of Tumours of Haematopoietic and Lymphoid Tissues;Swerdlow,2017
2. Treatment of multiple myeloma with high-risk cytogenetics: a consensus of the International Myeloma Working Group;Sonneveld;Blood,2016
3. Requirements For Cytogenetic Testing,2013
4. An integrative framework for the identification of double minute chromosomes using next generation sequencing data;Hayes;BMC Genet,2015
5. Double minute chromosomes in acute myeloid leukemia, myelodysplastic syndromes, and chronic myelomonocytic leukemia are associated with micronuclei, MYC or MLL amplification, and complex karyotype;Huh;Cancer Genet,2016
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