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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906304/
https://www.ncbi.nlm.nih.gov/pubmed/31827071
http://dx.doi.org/10.1038/s41408-019-0264-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906304/
https://www.ncbi.nlm.nih.gov/pubmed/31827071
http://dx.doi.org/10.1038/s41408-019-0264-y

Ejemplares similares