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

Recent genomic research efforts in multiple myeloma have revealed clinically relevant molecular subgroups beyond conventional cytogenetic classifications. Implementing these advances in clinical trial design and in routine patient care requires a new generation of molecular diagnostic tools. Here, w...

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Detalhes bibliográficos
Publicado no:Blood Cancer J
Main Authors: Yellapantula, Venkata, Hultcrantz, Malin, Rustad, Even H., Wasserman, Ester, Londono, Dory, Cimera, Robert, Ciardiello, Amanda, Landau, Heather, Akhlaghi, Theresia, Mailankody, Sham, Patel, Minal, Medina-Martinez, Juan Santiago, Arango Ossa, Juan Esteban, Levine, Max Fine, Bolli, Niccolo, Maura, Francesco, Dogan, Ahmed, Papaemmanuil, Elli, Zhang, Yanming, Landgren, Ola
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6906304/
https://ncbi.nlm.nih.gov/pubmed/31827071
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41408-019-0264-y
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