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Clonal diversity of recurrently mutated genes in myelodysplastic syndromes
Recent studies suggest that most cases of myelodysplastic syndrome (MDS) are clonally heterogeneous, with a founding clone and multiple subclones. It is not known whether specific gene mutations typically occur in founding clones or subclones. We screened a panel of 94 candidate genes in a cohort of...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
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2013
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3736571/ https://ncbi.nlm.nih.gov/pubmed/23443460 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/leu.2013.58 |
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