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Leukemia Research
Volume 34, Issue 4
, Pages 418-419
, April 2010
Pediatric acute lymphoblastic leukemia: There is no TEL-ing what wonders lie ahead
References
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- Uniform approach to risk classification and treatment assignment for children with acute lymphoblastic leukemia. J Clin Oncol. 1996;14:18–24
- High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood. 1995;86:4263–4269
- Prenatal origin of acute lymphoblastic leukaemia in children. Lancet. 1999;354:1499–1503
- . TEL-AML1 fusion precedes differentiation to pre-B cells in childhood acute lymphoblastic leukemia. Leuk Res. 2003;27:155–164
- Chromosome 12p deletions in TEL-AML1 childhood acute lymphoblastic leukemia are associated with retrotransposon elements and occur postnatally. Cancer Res. 2008;68:9935–9944
- TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. Leukemia. 1995;9:1985–1989
- CD9 expression can be used to predict childhood TEL/AML 1-positive acute lymphoblastic leukemia: proposal for an accelerated diagnostic flowchart. Leuk Res. 2010;34:430–437
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PII: S0145-2126(09)00502-5
doi: 10.1016/j.leukres.2009.10.009
© 2009 Elsevier Ltd. All rights reserved.
« Previous
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Leukemia Research
Volume 34, Issue 4
, Pages 418-419
, April 2010
