Mutations and karyotype in myelodysplastic syndromes: TP53 clusters with monosomal karyotype, RUNX1 with trisomy 21, and SF3B1 with inv(3)(q21q26.2) and del(11q)

Detalles Bibliográficos
Autores principales: Tefferi, Ayalew, Idossa, Dame, Lasho, Terra L., Mudireddy, Mythri, Finke, Christy, Shah, Sahrish, Nicolosi, Maura, Patnaik, Mrinal M., Pardanani, Animesh, Gangat, Naseema, Hanson, Curt A., Ketterling, Rhett P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802462/
https://www.ncbi.nlm.nih.gov/pubmed/29249799
http://dx.doi.org/10.1038/s41408-017-0017-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802462/
https://www.ncbi.nlm.nih.gov/pubmed/29249799
http://dx.doi.org/10.1038/s41408-017-0017-8

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