Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion

The rare but recurrent RUNX1-USP42 fusion gene is the result of a t(7;21)(p22;q22) chromosomal translocation and has been described in 6 cases of acute myeloid leukemia (AML) and one case of refractory anemia with excess of blast. In the present study, we present the molecular genetic analysis and t...

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Detaylı Bibliyografya
Asıl Yazarlar: PANAGOPOULOS, IOANNIS, GORUNOVA, LUDMILA, BRANDAL, PETTER, GARNES, MARGARET, TIERENS, ANNE, HEIM, SVERRE
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: D.A. Spandidos 2013
Konular:
Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3810351/
https://ncbi.nlm.nih.gov/pubmed/23877199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/or.2013.2623
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