-
1
-
-
6344289461
-
Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukaemia: An interphase FISH analysis
-
Attarbaschi, A., Mann, G., König, M., Dworzak, M.N., Trebo, M.M., Mühlegger, N., Gadner, H. & Haas, O.A. (2004) Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukaemia: an interphase FISH analysis. Leukemia, 18, 1611-1616.
-
(2004)
Leukemia
, vol.18
, pp. 1611-1616
-
-
Attarbaschi, A.1
Mann, G.2
König, M.3
Dworzak, M.N.4
Trebo, M.M.5
Mühlegger, N.6
Gadner, H.7
Haas, O.A.8
-
2
-
-
0030742017
-
Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials
-
Borkhardt, A., Cazzaniga, G., Viehmann, S., Valsecchi, M.G., Ludwig, W.D., Burci, L., Mangioni, S., Schrappe, M., Riehm, H., Lampert, F., Basso, G., Masera, G., Harbott, J. & Biondi, A. (1997) Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Blood, 90, 571-577.
-
(1997)
Blood
, vol.90
, pp. 571-577
-
-
Borkhardt, A.1
Cazzaniga, G.2
Viehmann, S.3
Valsecchi, M.G.4
Ludwig, W.D.5
Burci, L.6
Mangioni, S.7
Schrappe, M.8
Riehm, H.9
Lampert, F.10
Basso, G.11
Masera, G.12
Harbott, J.13
Biondi, A.14
-
3
-
-
0004783768
-
Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries
-
Forestier, E., Johansson, B., Borgström, G., Kerndrup, G., Johannsson, J. & Heim, S. (2000) Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. European Journal of Haematology, 64, 194-200.
-
(2000)
European Journal of Haematology
, vol.64
, pp. 194-200
-
-
Forestier, E.1
Johansson, B.2
Borgström, G.3
Kerndrup, G.4
Johannsson, J.5
Heim, S.6
-
4
-
-
0034667267
-
TEL/AML1 fusion gene: Its frequency and prognostic significance in childhood acute lymphoblastic leukemia
-
Jamil, A., Theil, K.S., Kahwash, S., Ruyman, F.B. & Klopfenstein, K.J. (2000) TEL/AML1 fusion gene: its frequency and prognostic significance in childhood acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics, 122, 73-78.
-
(2000)
Cancer Genetics and Cytogenetics
, vol.122
, pp. 73-78
-
-
Jamil, A.1
Theil, K.S.2
Kahwash, S.3
Ruyman, F.B.4
Klopfenstein, K.J.5
-
5
-
-
0032907413
-
Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukaemia with TEL/AML1 gene fusion
-
Loncarevic, I.F., Roitzheim, B., Ritterbach, J., Viehmann, S., Borkhardt, A., Lampert, F. & Harbott, J. (1999) Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukaemia with TEL/AML1 gene fusion. Genes, Chromosomes and Cancer, 24, 272-277.
-
(1999)
Genes, Chromosomes and Cancer
, vol.24
, pp. 272-277
-
-
Loncarevic, I.F.1
Roitzheim, B.2
Ritterbach, J.3
Viehmann, S.4
Borkhardt, A.5
Lampert, F.6
Harbott, J.7
-
6
-
-
0007055492
-
TEL/AML1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia
-
McLean, T.W., Ringold, S., Neuberg, D., Stegmeier, K., Tantravahi, R., Ritz, J., Koeffler, P.H., Takeuchi, S., Janssen, J.W.G., Seriu, T., Bartram, C.R., Sallan, S.E., Gilliland, G.D. & Golub, T.R. (1996) TEL/AML1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia. Blood, 88, 4252-4258.
-
(1996)
Blood
, vol.88
, pp. 4252-4258
-
-
McLean, T.W.1
Ringold, S.2
Neuberg, D.3
Stegmeier, K.4
Tantravahi, R.5
Ritz, J.6
Koeffler, P.H.7
Takeuchi, S.8
Janssen, J.W.G.9
Seriu, T.10
Bartram, C.R.11
Sallan, S.E.12
Gilliland, G.D.13
Golub, T.R.14
-
8
-
-
24944520140
-
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson, K., Mörse, H., Fioretos, T., Behrendtz, M., Strömbeck, B. & Johansson, B. (2005) Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia. Genes Chromosomes and Cancer, 44, 113-122.
-
(2005)
Genes Chromosomes and Cancer
, vol.44
, pp. 113-122
-
-
Paulsson, K.1
Mörse, H.2
Fioretos, T.3
Behrendtz, M.4
Strömbeck, B.5
Johansson, B.6
-
9
-
-
0026537436
-
Trisomy 21 as the sole acquired chromosomal abnormality in children with acute lymphoblastic leukemia
-
Raimondi, S.C., Pui, C-H., Head, D., Behm, F., Privitera, E., Robertson, P.K., Rivera, G.K. & Williams, D.L. (1992) Trisomy 21 as the sole acquired chromosomal abnormality in children with acute lymphoblastic leukemia. Leukemia, 6, 171-175.
-
(1992)
Leukemia
, vol.6
, pp. 171-175
-
-
Raimondi, S.C.1
Pui, C.-H.2
Head, D.3
Behm, F.4
Privitera, E.5
Robertson, P.K.6
Rivera, G.K.7
Williams, D.L.8
-
10
-
-
0032841521
-
Cytogenetic abnormalities associated with the t(12;21): A collaborative study of 169 children with t(12;21)-positive acute lymphoblastic leukemia
-
Raynaud, S.D., Dastugue, N., Zoccola, D., Shurtleff, S.A., Mathew, S. & Raimondi, S.C. (1999) Cytogenetic abnormalities associated with the t(12;21): a collaborative study of 169 children with t(12;21)-positive acute lymphoblastic leukemia. Leukemia, 13, 1325-1330.
-
(1999)
Leukemia
, vol.13
, pp. 1325-1330
-
-
Raynaud, S.D.1
Dastugue, N.2
Zoccola, D.3
Shurtleff, S.A.4
Mathew, S.5
Raimondi, S.C.6
-
11
-
-
0027420675
-
Trisomy 21 in childhood acute lymphoblastic leukemia: A pediatric oncology group study (8602)
-
Watson, M.S., Carroll, A.J., Shuster, J.J., Steuber, C.P., Borowitz, M.J., Behm, F.G., Pullen, D.J. & Land, V.J. (1993) Trisomy 21 in childhood acute lymphoblastic leukemia: a pediatric oncology group study (8602). Blood, 82, 3098-3102.
-
(1993)
Blood
, vol.82
, pp. 3098-3102
-
-
Watson, M.S.1
Carroll, A.J.2
Shuster, J.J.3
Steuber, C.P.4
Borowitz, M.J.5
Behm, F.G.6
Pullen, D.J.7
Land, V.J.8
|