Typical CBFβ/MYH11 fusion due to insertion of the 3′-MYH11 gene into 16q22 in acute monocytic leukemia with normal chromosomes 16 and trisomies 8 and 22

Author:

Aventı́n Anna,La Starza Roberta,Nomdedéu Josep,Brunet Salut,Sierra Jorge,Mecucci Cristina

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference10 articles.

1. Frequency of CBFβ/MYH11 fusion transcripts in patients entered into the U.K. MRC AML trials;Langabeer;Br J Haematol,1997

2. Detection of karyotypic aberrations in acute myeloblastic leukaemia;Krauter;Br J Haematol,1998

3. Characterization of cryptic rearrangements and variant translocations in acute promyelocytic leukemia;Grinwade;Blood,1997

4. Simple variant t(8;21) acute myeloid leukemias harbor insertions of the AML1 or ETO genes;Taviaux;Genes Chromosom Cancer,1999

5. Trisomy 22—A new abnormality found in acute leukemia characterized by eosinophilia and monocytoid blasts expressing immature differentiation;Najfeld;Cancer Genet Cytogenet,1986

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