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The clinical implications of gene mutations in chronic lymphocytic leukaemia
Chronic lymphocytic leukaemia (CLL) is a molecularly heterogeneous disease as revealed by recent genomic studies. Among genetic lesions that are recurrent in CLL, few clinically validated prognostic markers, such as TP53 mutations and 17p deletion, are available for the use in clinical practice to g...
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| Foilsithe in: | Br J Cancer |
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| Main Authors: | , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Nature Publishing Group
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4984803/ https://ncbi.nlm.nih.gov/pubmed/27031852 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/bjc.2016.78 |
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