Abnormalities of the der(12)t(12;21) in ETV6‐RUNX1 acute lymphoblastic leukemia
Author:
Affiliation:
1. Leukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle‐upon‐Tyne, UK
Publisher
Wiley
Subject
Cancer Research,Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22021
Reference41 articles.
1. Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia
2. Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: an interphase FISH analysis
3. Deletion size characterization of der(9) deletions in Philadelphia-positive chronic myeloid leukemia
4. Cytogenetic patterns inETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature
5. Large deletions 5′ to the ETO breakpoint are recurrent events in patients with t(8;21) acute myeloid leukemia
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