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  • 1
    Rowley JD: Chromosome abnormalities in cancer. Cancer Genetics and Cytogenetics 2: 175198, 1980.
  • 2
    McKusick VA, Ruddle FH: The status of the gene map of the human chromosomes. Science 196: 390405, 1977.
  • 3
    Croce CM, Shander M, Martinis J, et al: Chromosomal location of the genes for human immunoglobulin heavy chains. Proc Natl Acad Sci USA 76: 34163419, 1979.
  • 4
    First International Workshop on Chromosomes in Leukemia: Chromosomes in acute non-lymphocytic leukemia. Br J Haematol 39: 311316, 1978.
  • 5
    Second International Workshop on Chromosomes in Leukemia (1979): General report. Cancer Genetics and Cytogenetics 2: 9396, 1980.
  • 6
    International System for Human Cytogenetic Nomenclature, in Birth Defects, Original Article Series, vol 14. New York, The National Foundation—March of Dimes, 1978. Also in, Cytogenet Cell Genet 21: 309404, 1978.
  • 7
    FraumeniJFJr (ed): Persons at High Risk of Cancer: An Approach to Cancer Etiology and Control. New York, Academic Press Inc, 1975.
  • 8
    Kurita S, Kamei Y, Ota K: Genetic studies on familial leukemia. Cancer 34: 10981101, 1974.
  • 9
    Kaneko Y, Rowley JD, Variakojis D, et al: Chromosome abnormalities in Down's syndrome patients with acute leukemia. Blood, to be published.
  • 10
    Heath CW Jr: Hereditary factors in leukemia and lymphoma, in LynchHT (ed): Cancer Generics. Springfield, Ill, Charles C Thomas Publisher, 1976.
  • 11
    Hecht F, McCaw BK: Chromosome instability syndromes, in MulvihillJJ, MillerRW, FraumeniJFJr (eds): Genetics of Human Cancer. New York, Raven Press, 1977.
  • 12
    German J: Genes which increase chromosomal instability in somatic cells and predispose to cancer. Prog Med Genet 8: 61101, 1972.
  • 13
    Friedberg EC, Ehmann UK, Williams JI: Human diseases associated with defective DNA repair. Adv Rad Biol 8: 85174, 1979.
  • 14
    Nowell PC, Hungerford DA: A minute chromosome in human chronic granulocytic leukemia. Science 132: 1197, 1960.
  • 15
    Caspersson T, Gahrton G, Lindsten J, et al: Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis. Exp Cell Res 63: 238240, 1970.
  • 16
    O'Riordan ML, Robinson JA, Buckton KE, et al: Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and chronic myeloid leukaemia (Phmath image) by fluorescence. Nature 230: 167168, 1971.
  • 17
    Rowley JD: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining, letter. Nature 243: 290293, 1973.
  • 18
    Mayall BH, Carrano AV, Moore DH II, et al: Quantification by DNA-based cytophotometry of the 9q + /22q – chromosomal translocation associated with chronic myelogenous leukemia. Cancer Res 37: 35903593, 1977.
  • 19
    Fialkow PJ, Jacobson RJ, Papayannopoulou T: Chronic myelocytic leukemia: clonal origin in a stem cell common to the granulocyte, erythrocyte, platelet, and monocyte/macrophage. Am J Med 63: 125130, 1977.
  • 20
    Fitzgerald PH, Pickering AF, Eiby JR: Clonal origin of the Philadelphia chromosome and chronic myeloid leukaemia: evidence from a sex chromosome mosaic. Br J Haematol 21: 473480, 1971.
  • 21
    Rowley JD: Phmath image-positive leukaemia, including chronic myelogenous leukaemia. Clin Haematol 9: 5586, 1980.
  • 22
    Mitelman F: Heterogeneity of Phmath image in chronic myeloid leukaemia. Hereditas 76: 315316, 1974.
  • 23
    Sonta S, Oshimura M, Sandberg AA: Chromosomes and causation of human cancer and leukemia. XXI. Cytogenetically unusual cases of leukemia. Blood 48: 697705, 1976.
  • 24
    Bloomfield CD, Lindquist LL, Brunning RD, et al: The Philadelphia chromosome in acute leukemia. Virchows Arch [Cell Pathol] 29: 8191, 1978.
  • 25
    Whang-Peng J, Canellos GP, Carbone PP, et al: Clinical implications of cytogenetic variants in chronic myelocytic leukemia (CML). Blood 32: 755766, 1968.
  • 26
    Krompotic E, Lewis JP, Donnelly WJ: Chromosome aberrations in two patients with chronic granulocytic leukemia undergoing acute transformation. Am J Clin Pathol 49: 161170, 1968.
  • 27
    Alimena G, Brandt L, Dallapiccola B, et al: Secondary chromosome changes in chronic myeloid leukemia: relation to treatment. Cancer Genetics and Cytogenetics 1: 7985, 1979.
  • 28
    Gall JA, Boggs DR, Chervenick PA, et al: Discordant patterns of chromosome changes and myeloblast proliferation during the terminal phase of chronic myeloid leukemia. Blood 47: 347353, 1976.
  • 29
    Strodes CH, Hyde EF, Pan SF, et al: Cytokinetic studies during remission of blastic crisis in a patient with chronic myelocytic leukemia. Scand J Haematol 10: 130135, 1973.
  • 30
    Cunningham I, Gee T, Dowling M, et al: Results of treatment of Phmath image(+) chronic myelogenous leukemia with an intensive treatment regimen (L-5 protocol). Blood 53: 375395, 1979.
  • 31
    Buckner CD, Stewart P, Clift RA, et al: Treatment of blastic transformation of chronic granulocytic leukemia by chemotherapy, total body irradiation, and infusion of cryopreserved autologous marrow. Exp Hematol 6: 96109, 1978.
  • 32
    Fefer A, Cheever MA, Thomas ED, et al: Disappearance of Phmath image-positive cells in four patients with chronic granulocytic leukemia after chemotherapy, irradiation, and marrow transplantation from an identical twin. N Engl J Med 300: 333337, 1979.
  • 33
    Bennett JM, Catovsky D, Daniel MT, et al: Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol 33: 451458, 1976.
  • 34
    Mitelman F, Brandt L, Nilsson PG: Relation among occupational exposure to potential mutagenic/carcinogenic agents, clinical findings, and bone marrow chromosomes in acute nonlymphocytic leukemia. Blood 52: 12291237, 1978.
  • 35
    Rowley JD: Chromosome changes in acute leukaemia. Br J Haematol 44: 339346, 1980.
  • 36
    Borgström GH, Teerenhovi L, Vuopio P, et al: Clinical implications of monosomy 7 in acute nonlymphocytic leukemia. Cancer Genetics and Cytogenetics 2: 115126, 1980.
  • 37
    Ruutu P, Ruutu T, Vuopie P, et al: Defective chemotaxis in monosomy 7. Nature 265: 146147, 1977.
  • 38
    Golomb HM, Vardiman JW, Rowley JD: Acute nonlymphocytic leukemia in adults: correlations with Q-banded chromosomes. Blood 48: 921, 1976.
  • 39
    Golomb HM, Vardiman JW, Rowley JD, et al: Correlation of clinical findings with quinacrine-banded chromosomes in 90 adults with acute nonlymphocytic leukemia: an eight-year study (1970–1977). N Engl J Med 299: 613619, 1978.
  • 40
    Testa JR, Mintz U, Rowley JD, et al: Evolution of karyotypes in acute nonlymphocytic leukemia. Cancer Res 39: 36193627, 1979.
  • 41
    Second International Workshop on Chromosomes in Leukemia (1979): Cytogenetic, morphologic, and clinical correlations in acute nonlymphocytic leukemia with t(8q–;21q +). Cancer Genetics and Cytogenetics 2: 99102, 1980.
  • 42
    Golomb HM, Testa JR, Vardiman JW, et al: Cytogenetic and ultrastructural features of de novo acute promyelocytic leukemia: The University of Chicago experience (1973–1978). Cancer Genetics and Cytogenetics 1: 6978, 1979.
  • 43
    Golomb HM, Rowley JD, Vardiman JW, et al: “Microgranular” acute promyelocytic leukemia: a distinct clinical, ultrastructural, and cytogenetic entity. Blood 55: 253259, 1980.
  • 44
    Second International Workshop on Chromosomes in Leukemia (1979): Chromosomes in acute promyelocytic leukemia. Cancer Genetics and Cytogenetics 2: 103107, 1980.
  • 45
    Carbonell F, Fliedner TM, Kratt E, et al: Crecimiento de las células leucémicas en cultivo: selección de clones citogenéticamente anormales. Sangre 24: 10571060, 1979.
  • 46
    Bennett JM, Catovsky D, Daniel MT, et al: French-American-British (FAB) cooperative group. A variant form of hypergranular promyelocytic leukemia (M3). Ann Intern Med 92: 261, 1980.
  • 47
    Jones ME, Saleem A: Acute promyelocytic leukemia. A review of literature. Am J Med 65: 673677, 1978.
  • 48
    Drapkin RL, Gee TS, Dowling MD, et al: Prophylactic heparin therapy in acute promyelocytic leukemia. Cancer 41: 24842490, 1978.
  • 49
    Auclerc G, Jacquillat C, Auclerc MF, et al: Post-therapeutic acute leukemia. Cancer 44: 20172025, 1979.
  • 50
    Cadman EC, Capizzi RL, Bertino JR: Acute nonlymphocytic leukemia. A delayed complication of Hodgkin's disease therapy: analysis of 109 cases. Cancer 40: 12801296, 1977.
  • 51
    Coleman CN, Williams CJ, Flint A, et al: Hematologic neoplasia in patients treated for Hodgkin's disease. N Engl J Med 297: 12491252, 1977.
  • 52
    Vardiman JW, Golomb HM, Rowley JD, et al: Acute nonlymphocytic leukemia in malignant lymphoma: a morphologic study. Cancer 42: 229242, 1978.
  • 53
    Reimer RR, Hoover R, Fraumeni JF Jr, et al: Acute leukemia after alkylating-agent therapy of ovarian cancer. N Engl J Med 297: 177181, 1977.
  • 54
    Bergsagel DE, Bailey AJ, Langley GR, et al: The chemotherapy of plasma-cell myeloma and the incidence of acute leukemia. N Engl J Med 301: 743748, 1979.
  • 55
    Preisler HD, Lyman GH: Acute myelogenous leukemia subsequent to therapy for a different neoplasm: clinical features and response to therapy. Am J Hematol 3: 209218, 1977.
  • 56
    Rowley JD, Golomb HM, Vardiman JW: Nonrandom chromosomal abnormalities in acute nonlymphocytic leukemia in patients treated for Hodgkin's disease and non-Hodgkin's lymphoma. Blood 50: 759770, 1977.
  • 57
    Rowley JD, Golomb HM, Vardiman JW: Nonrandom chromosome abnormalities in secondary acute leukemia: relevance to etiology of ANLL de novo. Submitted for publication, 1981.
  • 58
    Casciato DA, Scott JL: Acute leukemia following prolonged cytotoxic agent therapy. Medicine 58: 3247, 1979.
  • 59
    Third International Workshop on Chromosomes in Acute Leukemia (1980): Clinical significance of chromosomal abnormalities in acute lymphoblastic leukemia, abstracted. Proceedings of the American Society of Clinical Oncology 22: 477, 1981.
  • 60
    Rowley JD: Chromosome abnormalities in acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics 1: 263271, 1980.
  • 61
    Gahrton G, Robèrt KH, Friberg K, et al: Extra chromosome 12 in chronic lymphocytic leukaemia. Lancet 1: 146147, 1980.
  • 62
    Gahrton G, Zech L, Robèrt KH, et al: Mitogenic stimulation of leukemia cells by Epstein-Barr virus, letter. N Engl J Med 301: 438439, 1979.
  • 63
    Autio K, Turunen O, Penttilä O, et al: Human chronic lymphocytic leukemia. Karyotypes in different lymphocyte populations. Cancer Genetics and Cytogenetics 1: 147155, 1979.
  • 64
    Liang W, Hopper JE, Rowley JD: Karyotypic abnormalities and clinical aspects of patients with multiple myeloma and related paraproteinemic disorders. Cancer 44: 630644, 1979.
  • 65
    Rowley JD, Fukuhara S: Chromosome studies in non-Hodgkin's lymphomas. Semin Oncol 7: 255266, 1980.
  • 66
    Manolov G, Manolova Y: Marker band in one chromosome 14 from Burkitt lymphomas. Nature 237: 3334, 1972.
  • 67
    Zech L, Haglund U, Nilsson K, et al: Characteristic chromosomal abnormalities in biopsies and lymphoid-cell lines from patients with Burkitt and non-Burkitt lymphomas. Int J Cancer 17: 4756, 1976.
  • 68
    Miyoshi I, Hiraki S, Kimura I, et al: 2/8 translocation in a Japanese Burkitt's lymphoma. Experientia 35: 742743, 1979.
  • 69
    Berger R, Bernheim A, Weh HJ, et al: A new translocation in Burkitt's tumor cells. Hum Genet 53: 111112, 1979.
  • 70
    McCaw BK, Epstein AL, Kaplan HS, et al: Chromosome 14 translocation in African and North American Burkitt's lymphoma. Int J Cancer 19: 482486, 1977.
  • 71
    Fukuhara S, Rowley JD, Variakojis D, et al: Banding studies on chromosomes in diffuse “histiocytic” lymphomas: correlation of 14q + marker chromosome with cytology. Blood 52: 9891002, 1978.
  • 72
    Kaneko Y, Rowley JD, Check I, et al: The 14q + chromosome in pre-B-ALL. Blood 56: 782785, 1980.
  • 73
    McCaw BK, Hecht F, Harnden DG, et al: Somatic rearrangement of chromosome 14 in human lymphocytes. Proc Natl Acad Sci USA 72: 20712075, 1975.
  • 74
    Rowley JD: Mapping of human chromosomal regions related to neoplasia: evidence from chromosomes 1 and 17. Proc Natl Acad Sci USA 74: 57295733, 1977.
  • 75
    Owerbach D, Doyle D, Shows TB: Genetics of the large external, transformation-sensitive (LETS) protein: assignment of a gene coding for expression of LETS to human chromosome 8. Proc Natl Acad Sci USA 75: 56405644, 1978.