Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma

V. Yellapantula, M. Hultcrantz, E.H. Rustad, E. Wasserman, D. Londono, R. Cimera, A. Ciardiello, H. Landau, T. Akhlaghi, S. Mailankody, M. Patel, J.S. Medina-Martinez, J.E. Arango Ossa, M.F. Levine, N. Bolli, F. Maura, A. Dogan, E. Papaemmanuil, Y. Zhang, O. Landgren

Research output: Contribution to journalArticle

Original languageEnglish
JournalBlood Cancer Journal
Volume9
Issue number12
DOIs
Publication statusPublished - 2019

Cite this

Yellapantula, V., Hultcrantz, M., Rustad, E. H., Wasserman, E., Londono, D., Cimera, R., Ciardiello, A., Landau, H., Akhlaghi, T., Mailankody, S., Patel, M., Medina-Martinez, J. S., Arango Ossa, J. E., Levine, M. F., Bolli, N., Maura, F., Dogan, A., Papaemmanuil, E., Zhang, Y., & Landgren, O. (2019). Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma. Blood Cancer Journal, 9(12). https://doi.org/10.1038/s41408-019-0264-y