Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia
Golub TR, Barker GF, Bohlander SK, et al. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc Natl Acad Sci USA 1995; 92:4917-21.
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 SA, Buijs A, Behm FG, et al. 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; 9:1985-9.
Genetic studies of childhood acute lymphoblastic leukemia with emphasis on p16, MLL and ETV6 gene abnormalities: Results of St. Jude Total Therapy Study XII
Rubnitz JE, Behm FG, Pui CH, et al. Genetic studies of childhood acute lymphoblastic leukemia with emphasis on p16, MLL and ETV6 gene abnormalities: results of St. Jude Total Therapy Study XII. Leukemia 1997; 11:1201-6.
p16(INK4a) gene inactivation by deletions, mutations, and hypermethylation is associated with transformed and aggressive variants of non-Hodgkin's lymphomas
Pinyol M, Cobo F, Bea S, et al. p16(INK4a) gene inactivation by deletions, mutations, and hypermethylation is associated with transformed and aggressive variants of non-Hodgkin's lymphomas. Blood 1998; 91:2977-84.
Low frequency of the TEL/AML1 fusion gene in acute lymphoblastic leukaemia in Spain
Garcia-Sanz R, Alaejos I, Orfao A, et al. Low frequency of the TEL/AML1 fusion gene in acute lymphoblastic leukaemia in Spain. Br J Haematol 1999; 107:667-9.
TEL/AML1 transcript and p16 gene deletion in a patient with childhood acute lymphoblastic leukaemia
Anguita E, González FA, López J, Villegas A. TEL/AML1 transcript and p16 gene deletion in a patient with childhood acute lymphoblastic leukaemia. Br J Haematol 1997; 99: 240-1.