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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...

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Detaylı Bibliyografya
Asıl Yazarlar: Kreuziger, Lisa M. Baumann, Porcher, Julie Cliff, Ketterling, Rhett P., Steensma, David P.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2007
Konular:
Online Erişim: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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