Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes

To explore novel genetic abnormalities occurring in myelodysplastic syndromes (MDS) through an integrative study combining array-based comparative genomic hybridization (aCGH) and next-generation sequencing (NGS) in a series of MDS and MDS/myeloproliferative neoplasms (MPN) patients. 301 patients di...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Abáigar, María, Robledo, Cristina, Benito, Rocío, Ramos, Fernando, Díez-Campelo, María, Hermosín, Lourdes, Sánchez-del-Real, Javier, Alonso, Jose M., Cuello, Rebeca, Megido, Marta, Rodríguez, Juan N., Martín-Núñez, Guillermo, Aguilar, Carlos, Vargas, Manuel, Martín, Ana A., García, Juan L., Kohlmann, Alexander, del Cañizo, M. Consuelo, Hernández-Rivas, Jesús M.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5065168/
https://ncbi.nlm.nih.gov/pubmed/27741277
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0164370
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