References
- Rowley J. Recurring chromosomal abnormalities in leukemia and lymphoma. Semin Hematol 1990; 27: 122–236
- Rubin C M, Rowley J D. Chromosomal abnormalities in childhood malignant disease. Hematology of Infancy and Childhood. 4th ed., D G Nathan, F A Oski. Saunders WB, Philadelphia 1993; 1179–1206
- Raimondi S C. Current status of cytogenetic research in childhood acute lymphoblastic leukemia. Blood 1993; 9: 2237–51
- McAlpine P J, Shows T B, Boucheix C, Pericak-Vance M A, Anderson W A. The 1992 Catalog of Mapped Genes and Report of the Nomenclature Committee; Chromosome Coordinating Meeting (1992). Genome Priority Reports, Vol. 1, A J Cuticchia, P L Pearson, H P Klinger. Karger, Basel 1993; 11–142
- Sixth International Workshop on Chromosomes in Leukemia. Cancer Genet Cytogenet 1989; 40: 141–230
- Rowley J D. Involvement of the MLL gene in 11q23 translocations. Seminars in Cancer Biology, T H Rabbitts. Academic Press, London 1993, in press.
- Cimino G, Moir D T, Canaani O, et al. Cloning of ALL-1, the locus involved in leukemias with the t(4;11) (q21;q23), t(9;11) (p22;q23), and t(11;19) (q23;p13) chromosome translocations. Cancer Res 1991; 51: 6712–14
- Djabali M, Selleri L, Parry P, Bower M, Young B D, Evans G A. A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias. Nature Genet 1992; 2: 113–8
- Tkachuk D C, Kohler S, Cleary M L. Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias. Cell 1992; 71: 691–700
- Thirman M J, Gill H J, Burnett R C, et al. A cDNA probe detects all rearrangements of the MLL gene in leukemias with common and rare 11q23 translocations. N Engl J Med 1993; 329: 909–14
- Ratain M J, Rowley J D. Therapy-related acute myeloid leukemia secondary to inhibitors of topoisomerase. II: From the bedside to the target genes. Ann Oncol 1992; 3: 107–11
- Chen C-S, Sorensen PH B, Domer P H, et al. Molecular rearrangements on chromosome 11q23 predominant in infant acute lymphoblastic leukemia are associated with specific biologic variables and poor outcome. Blood 1993; 9: 2386–93
- Sorenson PH B, Smith F O, Chen C-S, et al. Molecular rearrangements of chromosome band 11q23 are present in most cases of infant AML and are strongly correlated with monocytic or myelomonocytic phenotype. J. Clin. Invest, in press.
- Hunger S P, Galili N, Carroll A J, Crist W M, Link M P, Cleary M L. The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias. Blood 1991; 77: 687–93
- 1984; 11: 249–360
- Bennett J M, Catovsky D, Daniel M T, et al. Proposed revised criteria for the classification of acute myeloid leukemia: A report of the French-American-British Cooperative Group. Ann Intern Med 1985; 103: 626–29
- Bitter M A, Le Beau M M, Rowley J D, et al. Associations between morphology, karyotype, and clinical features in myeloid leukemias. Hum Pathol 1987; 18: 211–25
- Erickson P, Gao J, Chang K S, et al. Detection of AML t(8;21) breakpoints and a fusion transcript with similarity to Drosophila segmentation gene, runt. Blood 1992; 80: 1825–31
- Nucifora G, Birn D J, Erickson P, et al. Detection of DNA rearrangements in the AML1 and ETO loci and of an AML1/ETO fusion mRNA in patients with t(8;21) AML. Blood 1993; 81: 883–8
- Solomon E, Borrow J, Goddard A D. Chromosome aberrations and cancer. Science 1991; 254: 1153–60
- Warrell R P, Jr, de Thé H, Wang Z-Y, Degos L. Acute promyelocytic leukemia. N Engl J Med 1993; 329: 177–89
- Huang M E, Yc Y C, Cliai J R, et al. Use of all trans-retinoic acid in treatment of acute promyelocytic leukemia. Blood 1988; 72: 567–72
- Kobayashi H, Espinosa R, III, Thirman M J, et al. Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization. Genes Chrom Cancer 1993; 7: 204–8
- Mitelman F. Catalog of Chromosome Aberrations in Cancer. 4th ed. Wiley-Liss, New York 1991
- Kovacs C T, Brusa P. Clonal chromosome aberrations in normal kidney tissue from patients with renal cell carcinoma. Cancer Genet Cytogenet 1989; 37: 289–90
- Fletcher J A, Kozakewich H P, Hoffer F A, et al. Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors. N Engl J Med 1991; 324: 436–42
- Delattre O, Zucman J, Plougastel B, et al. Gene fusion with an ETS DNA-binding domain caused by chromosome translocations in human tumors. Nature 1992; 359: 162–5
- Aman P, Ron D, Mandahl N, et al. Rearrangement of the transcriptor factor gene CHOP in myxoid liposarcomas with t(12;16) (q13;p11). Genes Chrom Cancer 1992; 5: 278–85
- Barr F G, Galili N, Holick J, Biegel J A, Rovera G, Emanuel B S. Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma. Nature Genet 1993; 3: 113–7
- Seeger R C, Brodeur G M, Sather H, et al. Association of multiple copies of N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med 1985; 313: 1111–6
- 1990s. [Workshop report of Institute of Medicine]. National Academy Press, Washington, DC 1992
- Rowley J D, Aster J C, Sklar J. The clinical applications of new DNA diagnostic technology on the management of cancer patients. JAMA 1993; 270, in press.