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An MLL-SEPT9 Fusion and t(11;17)(q23;q25) Associated With De Novo Myelodysplastic Syndrome
Rearrangements of the MLL gene at chromosome 11q23 are uncommon in de novo myelodysplastic syndrome (MDS). Here we describe molecular findings in a patient with multilineage dysplasia and t(11;17)(q23;q25) who responded to decitabine therapy. Fluorescent in situ hybridization (FISH) demonstrated rea...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2007
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2768487/ https://ncbi.nlm.nih.gov/pubmed/17250889 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.leukres.2006.12.006 |
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