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  • Andreasson, P., Höglund, M., Békássy, A.N., Garwicz, S., Heldrup, J., Mitelman, F. & Johansson, B. (2000) Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias. European Journal of Haematology, 65, 4051.
  • Autio, R., Hautaniemi, S., Kauraniemi, P., Yli-Harja, O., Astola, J., Wolf, M. & Kallioniemi, A. (2003) CGH-Plotter: MATLAB toolbox for CGH-data analysis. Bioinformatics, 19, 17141715.
  • Betts, D.R., Kingston, J.E., Dorey, E.L., Young, B.D., Webb, D., Katz, F.E. & Gibbons, B. (1990) Monosomy 20: a nonrandom finding in childhood acute lymphoblastic leukemia. Genes Chromosomes & Cancer, 2, 182185.
  • Busslinger, M. (2004) Transcriptional control of early B cell development. Annual Review of Immunology, 22, 5579.
  • Clark, R., Byatt, S.A., Bennett, C.F., Brama, M., Martineau, M., Moorman, A.V., Roberts, K., Secker-Walker, L.M., Richards, S., Eden, O.B., Goldstone, A.H. & Harrison, C.J. (2000) Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia. Leukemia, 14, 241246.
  • Heerema, N.A., Maben, K.D., Bernstein, J., Breitfeld, P.P., Neiman, R.S. & Vance, G.H. (1996) Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients. Cancer Genetics and Cytogenetics, 92, 111115.
  • Hupé, P., Stransky, N., Thiery, J. P., Radvanyi, F. & Barillot, E. (2004) Analysis of array CGH data: from signal ratio to gain and loss of DNA regions. Bioinformatics, 20, 34133422.
  • Johansson, B., Mertens, F. & Mitelman, F. (2004) Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia. Annals of Medicine, 36, 492503.
  • Jönsson, G., Bendahl, P.O., Sandberg, T., Kurbasic, A., Staaf, J., Sunde, L., Crüger, D.G., Ingvar, C., Olsson, H. & Borg, Å. (2005) Mapping of a novel ocular and cutaneous malignant melanoma susceptibility locus to chromosome 9q21.32. Journal of the National Cancer Institute, 97, 13771382.
  • Knight, S.J.L., Lese, C.M., Precht, K.S., Kuc, J., Ning, Y., Lucas, S., Regan, R., Brenan, M., Nicod, A., Lawrie, N.M., Cardy, D.L.N., Nguyen, H., Hudson, T.J., Riethman, H.C., Ledbetter, D.H. & Flint, J. (2000) An optimized set of human telomere clones for studying telomere integrity and architecture. American Journal of Human Genetics, 67, 320332.
  • Krzywinski, M., Bosdet, I., Smailus, D., Chiu, R., Mathewson, C., Wye, N., Barber, S., Brown-John, M., Chan, S., Chand, S., Cloutier, A., Girn, N., Lee, D., Masson, A., Mayo, M., Olson, T., Pandoh, P., Prabhu, A.L., Schoenmakers, E., Tsai, M., Albertson, D., Lam, W., Choy, C.O., Osoegawa, K., Zhao, S., De Jong, P.J., Schein, J., Jones, S. & Marra, M.A. (2004) A set of BAC clones spanning the human genome. Nucleic Acids Research, 32, 36513660.
  • Liu, X., Baker, E., Eyre, H.J., Sutherland, G.R. & Zhou, M. (1999) γ-Heregulin: a fusion gene of DOC-4 and neuregulin-1 derived from a chromosome translocation. Oncogene, 18, 71107114.
  • Mitelman, F., Johansson, B. & Mertens, F. (2006) Mitelman Database of Chromosome Aberrations in Cancer. http://cgap.nci.nih.gov/Chromosomes/Mitelman [accessed on 6 July 2006].
  • Nordgren, A., Heyman, M., Sahlén, S., Schoumans, J., Söderhäll, S., Nordenskjöld, M. & Blennow, E. (2002) Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 cases. European Journal of Haematology, 68, 3141.
  • Poppe, B., De Paepe, P., Michaux, L., Dastugue, N., Bastard, C., Herens, C., Moreau, E., Cavazzini, F., Yigit, N., Van Limbergen, H., De Paepe, A., Praet, M., De Wolf-Peeters, C., Wlodarska, I. & Speleman, F. (2005) PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B-NHL with complex chromosomal rearrangements. Genes Chromosomes & Cancer, 44, 218223.
  • Raimondi, S.C., Zhou, Y., Mathew, S., Shurtleff, S.A., Sandlund, J.T., Rivera, G.K., Behm, F.G. & Pui, C.H. (2003) Reassessment of the prognostic significance of hypodiploidy in pediatric patients with acute lymphoblastic leukemia. Cancer, 98, 27152722.
  • Rieder, H., Schnittger, S., Bodenstein, H., Schwonzen, M., Wörmann, B., Berkovic, D., Ludwig, W.D., Hoelzer, D. & Fonatsch, C. (1995) dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemia. Genes, Chromosomes & Cancer, 13, 5461.
  • Saal, L.H., Troein, C., Vallon-Christersson, J., Gruvberger, S., Borg, Å. & Peterson, C. (2002) BioArray Software Environment (BASE): a platform for comprehensive management and analysis of microarray data. Genome Biology, 3, software0003.1–software0003.6.
  • Schoumans, J., Staaf, J., Jönsson, G., Rantala, J., Zimmer, K.S., Borg, Å., Nordenskjöld, M. & Anderlid, B.M. (2005) Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to approximately 650 kb. European Journal of Medical Genetics, 48, 290300.
  • Silengo, M., Vassallo, E., Barisone, E., Miniero, R. & Madon, E. (1992) Monosomy 20 in childhood acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics, 59, 177179.
  • Slater, R., Smit, E., Kroes, W., Jotterand Bellomo, M., Mühlematter, D., Harbott, J., Behrendt, H., Hählen, K., Veerman, A.J.P. & Hagemeijer, A. (1995) A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11). Leukemia, 9, 16131619.
  • Strehl, S., König, M., Dworzak, M.N., Kalwak, K. & Haas, O.A. (2003) PAX5/ETV6 fusion defines cytogenetic entity dic(9;12)(p13;p13). Leukemia, 17, 11211123.
  • Vissers, L.E.L.M., De Vries, B.B.A., Osoegawa, K., Janssen, I.M., Feuth, T., Choy, C.O., Straatman, H., Van Der Vliet, W., Huys, E.H.L.P.G., Van Rijk, A., Smeets, D., Van Ravenswaaij-Arts, C.M.A., Knoers, N.V., Van Der Burgt, I., De Jong, P.J., Brunner, H.G., Geurts van Kessel, A., Schoenmakers, E.F.P.M. & Veltman, J.A. (2003) Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities. American Journal of Human Genetics, 73, 12611270.
  • Yang, Y.H., Dudoit, S., Luu, P., Lin, D.M., Peng, V., Ngai, J. & Speed, T.P. (2002) Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation. Nucleic Acids Research, 30, e15.