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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Detalles Bibliográficos
Autores principales: PANAGOPOULOS, IOANNIS, GORUNOVA, LUDMILA, BRANDAL, PETTER, GARNES, MARGARET, TIERENS, ANNE, HEIM, SVERRE
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810351/
https://www.ncbi.nlm.nih.gov/pubmed/23877199
http://dx.doi.org/10.3892/or.2013.2623

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810351/
https://www.ncbi.nlm.nih.gov/pubmed/23877199
http://dx.doi.org/10.3892/or.2013.2623

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