Involvement of der(12)t(12;21)(p13;q22) and as well as additional rearrangements of chromosome 12 homolog in ETV6/RUNX1-positive acute lymphoblastic leukemia

Author:

Stanchescu Racheli,Betts David R.,Rechavi Gideon,Amariglio Ninette,Trakhtenbrot Luba

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference30 articles.

1. Pui CH, Grosveld G, Downing JR. 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

2. TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia;McLean;Blood,1996

3. Fetal origins of the TEL-AML1 fusion gene in identical twins with leukemia;Ford;Proc Natl Acad Sci U S A,1998

4. Prenatal origin of acute lymphoblastic leukaemia in children;Wiemels;Lancet,1999

5. Cytogenetic abnormalities associated with the t(12;21): a collaborative study of 169 children with t(12;21)-positive acute lymphoblastic leukemia;Raynaud;Leukemia,1999

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