References
- Mauer AM. Acute lymphocytic leukemia, In: Williams W, Beutler E, Erslev A & Lichtman M. (eds) Hematology, 4th ed. New York: McGraw-Hill, 1990; 994.
- Nordgren A. Hidden aberrations diagnosed by interphase fluores-cence in situ hybridization and spectral karyotyping in childhood acute lymphoblastic leukaemia. Leuk Lymphoma 2003; 44: 2039–2053.
- Mitelman F, Mertens F, Johansson B. Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders. Genes Chromosomes Cancer 2005; 43: 350–366.
- Carbonell F, Swansbury J, Min T et al. Cytogenetic findings in acute biphenotypic leukaemia. Leukemia. 1996; 10: 1283–1287.
- Heerema N, Sather H, Sensel M et al. Frequency and clinical significance of cytogenetic abnormalities in pediatric T-lineage acute lymphoblastic leukemia: a report from the Children's Cancer Group. J Clin Oncol 1998; 16: 1270–1278.
- Chessells J, Harrison C, Kempski H et al. Clinical features, cytogenetics and outcome in acute lymphoblastic and myeloid leukaemia of infancy: report from the MRC childhood leukaemia working party. Leukemia 2002; 16: 776–784.
- Ribera J, Ortega J, Oriol A et al. Prognostic value of karyotypicanalysis in children and adults with high-risk acute lymphoblastic leukemia included in the PETHEMA ALL-93 trial. Haematologica 2002; 87: 154–166.
- Kansal R, Deeb G, Barcos M et al. Precursor B lymphoblastic leukemia with surface light chain immunoglobulin restriction: a report of 15 patients. Am J Clin Pathol 2004; 121: 512–525.
- Waghray M, Rowley J, Reddy P, Reddy S. A cytogenetic study ofchildren in India with acute lymphocytic leukemia: correlation with clinical data. Cancer Genet Cytogenet 1986; 23: 225–237.
- Gladstone B, Amare P, Pai S et al. Cytogenetic studies in patients from India with T-acute lymphoblastic leukemia. Cancer Genet Cytogenet 1998; 106: 44–48.
- Amare P, Gladstone B, Varghese C, Pai S, Advani S. Clinical significance of cytogenetic findings at diagnosis and in remission in childhood and adult acute lymphoblastic leukemia: experience from India. Cancer Genet Cytogenet 1999; 110: 44–53.
- Henegariu O, Heerema N, Lowe W, Bray-Ward P, Ward D, Vance G. Improvements in cytogenetic slide preparation: controlled chromosome spreading, chemical aging and gradual denaturing. Cytometry 2001; 43: 101–109.
- Chavan D, Ahmad F, Iyer P et al. Cytogenetic Investigation in Chronic Myeloid Leukemia: Study from an Indian Population. Asian Pacific Journal of Cancer Prevention 2006; 7: 423–426.
- Mitelman F. (ed) ISCN: An International System for Human Cytogenetic Nomenclature. Basel: Karger, 1995.
- Scandyra JM, Boccuni P, Cammenga J, Nimer SD. Transcription factor fusion in acute myeloid leukemia: variations on a theme. Oncogene 2002; 21: 3422–3444.
- Raimondi S, Zhou Y, Shurtleff S, Rubnitz J, Pui C, Behm F. Near-triploidy and near-tetraploidy in childhood acute lymphoblastic leukemia: association with B-lineage blast cells carrying the ETV6-RUNX1 fusion, T-lineage immunophenotype, and favorable outcome. Cancer Genet Cytogenet 2006; 169: 50–57.
- Gunzburg J. RAP2A. Atlas Genet Cytogenet Oncol Haematol, 2001; Available from: http://AtlasGeneticsOncology.org/Genes/RAP2AID274.html
- Marschalek R. AF4 (ALL] fused gene from chromosome 4); AFF1 (AF4IFMR2 family, member 1). Atlas Genet Cytogenet Oncol Haematol,2002; Availablefrom:http://AtlasGeneticsOncology.org/Genes/AF4.html
- Kahl C, Gesk S, Harder L et al. Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluores-cence in situ hybridization. Cancer Genet Cytogenet 2001; 129: 80–84.
- Russo G, Giordano A, Claudio P. RBL2 (retinoblastoma-like 2). Atlas Genet Cytogenet Oncol Haematol, 2004; Available from: http://AtlasGeneticsOncology.org/Genes/RBL2ID443.html
- Garipidou V, Yamada T, Prentice HG, Secker-Walker LM. Trisomy 8 in acute lymphoblastic leukemia (ALL): a case report and update of the literature. Leukemia 1990; 4: 717–719.
- Arana-Trejo R, Cervantes-Peredo A, Rozen E, Kassack J, Gutiérrez M, Kofman-Alfaro S. Estudio citogenético en 22 adultos y tres ninos con leucemia linfoblastica aguda. Rev Inv Clin 1993; 45: 43–48. Available: http://cgap.nci.nih.gov/Chromosomes/CytCaseInfo?REF=4920&CASE= 5
- Spirito FR, Mancini M, Derme V et al. Trisomy 13 in a patient with common acute lymphoblastic leukemia: description of a case and review of the literature. Cancer Genet Cytogenet 2003; 144: 69–72.
- Theodossiou C, Scalise A, Troy K, Silverman L, Perdahl-Wallace E, Najfeld V. Del(5q) in acute lymphoblastic leukemia with biphenotypic and early progenitor phenotype. Cancer Genet Cytogenet 1992; 63: 89–94.
- Pui CH, Cheng C, Leung W et al. Extended follow-up of long-termsurvivors of childhood acute lymphoblastic leukemia. N Engl J Med 2003; 349: 640–649.
- Bloomfield CD, Secker-Walker LM, Goldman Al et al. Six-year follow-up of the clinical significance of karyotype in acute lymphoblastic leukemia. Cancer Genet Cytogenet 1989; 40: 171–185.
- Secker-Walker LM, Alimena G, Bloomfield CD et al. Cytogenetic studies of 21 patients with acute lymphoblastic leukemia in relapse. Cancer Genet Cytogenet 1989; 40: 163–169.