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Examination of the FLT3 and NPM1 mutational status in patients with acute myeloid leukemia from southeastern Poland
INTRODUCTION: Acute myeloid leukemia (AML) is a genetically heterogeneous disease at both the cytogenetic and molecular levels. In AML cells many chromosomal aberrations are observed, some of them being characteristic of a particular subtype of patients, and others being less significant. Besides ch...
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| Publicat a: | Arch Med Sci |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Termedia Publishing House
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4754359/ https://ncbi.nlm.nih.gov/pubmed/26925127 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/aoms.2015.49811 |
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