Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia-Reference-Cited by-同舟云学术

Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia

Published:2005-10 Issue:1 Volume:162 Page:21-29
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Alvarez Y.,Coll M.D.,Ortega J.J.,Bastida P.,Dastugue N.,Robert A.,Cervera J.,Verdeguer A.,Tasso M.,Aventín A.,Guitart M.,Caballín M.R.

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference41 articles.

1. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia;Golub;Proc Natl Acad Sci U S A,1995

2. High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia;Romana;Blood,1995

3. 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;Shurtleff;Leukemia,1995

4. TEL gene rearrangement in acute lymphoblastic leukemia: a new genetic marker with prognostic significance;Rubnitz;J Clin Oncol,1997

5. TEL/AML1 fusion is a rare event in adult acute lymphoblastic leukemia;Raynaud;Leukemia,1996

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