Interphase FISH onTEL/AML1positive acute lymphoblastic leukemia relapses - analysis of clinical relevance of additionalTELandAML1copy number changes
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2009.01315.x/fullpdf
Reference67 articles.
1. The der(21)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia;Kobayashi;Br J Haematol,1996
2. ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia;Cave;Leukemia,1997
3. Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion;Loncarevic;Genes Chromosomes Cancer,1999
4. An investigation of the t(12;21) rearrangement in children with B-precursor acute lymphoblastic leukaemia using cytogenetic and molecular methods;Kempski;Br J Haematol,1999
5. Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: an interphase FISH analysis;Attarbaschi;Leukemia,2004
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2. Genetic Biomarkers and Their Clinical Implications in B-Cell Acute Lymphoblastic Leukemia in Children;International Journal of Molecular Sciences;2022-03-02
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