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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)
| Autores principales: | , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2017
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| Materias: | |
| 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 |
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| author | 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. |
| author_facet | 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. |
| author_sort | Tefferi, Ayalew |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-5802462 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | Nature Publishing Group UK |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-58024622018-02-08 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) 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. Blood Cancer J Correspondence Nature Publishing Group UK 2017-12-18 /pmc/articles/PMC5802462/ /pubmed/29249799 http://dx.doi.org/10.1038/s41408-017-0017-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
| spellingShingle | Correspondence 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. 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) |
| title | 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) |
| title_full | 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) |
| title_fullStr | 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) |
| title_full_unstemmed | 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) |
| title_short | 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) |
| title_sort | 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) |
| topic | Correspondence |
| url | 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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