Recurrent chromosomal defects are found in most patients with acute nonlymphocytic leukemia

Cancer Genetics and Cytogenetics - Tập 11 Số 2 - Trang 125-137 - 1984
Jorge J. Yunis1
1Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis, MN USA

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Tài liệu tham khảo

Sandberg, 1980

Yunis, 1981, New chromosome techniques in the study of human neoplasia, Human Pathol, 12, 540, 10.1016/S0046-8177(81)80068-8

Yunis, 1981, All patients with acute nonlymphocytic leukemia may have a chromosomal defect, N Engl J Med, 305, 135, 10.1056/NEJM198107163050304

Bennett, 1976, French-American-British (FAB) Cooperative Group proposals for the classification of acute leukemia, Br J Haematol, 33, 451, 10.1111/j.1365-2141.1976.tb03563.x

Yunis, 1982, Comparative analysis of high-resolution chromosome techniques for leukemic bone marrows, Cancer Genet Cytogenet, 7, 43, 10.1016/0165-4608(82)90106-6

1971

Yunis, 1981, Chromosomes and cancer: New nomenclature and future directions, Human Pathol, 12, 494, 10.1016/S0046-8177(81)80063-9

Sutherland, 1983, Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23,9p21,9q32, and 11q23, Am J Hum Genet, 35, 432

Pierre, 1972, Age-associated aneuploidy: Loss of Y chromosome from human bone marrow cells with aging, Cancer, 30, 889, 10.1002/1097-0142(197210)30:4<889::AID-CNCR2820300405>3.0.CO;2-1

Rowley, 1980, Chromosome changes in acute leukaemia, Br J Haematol, 44, 339, 10.1111/j.1365-2141.1980.tb05902.x

Mitelman, 1981, Clustering of aberrations to specific chromosomes in human neoplasias. IV. A survey of 1,871 cases, Hereditas, 95, 79, 10.1111/j.1601-5223.1981.tb01331.x

Yunis, 1983, High resolution chromosomes in the study of acute leukemias and non-Hodgkin's lymphomas

Carbonell, 1979, Crecimiento de las células leucémicas en cultivo: Selección de clones citogenéticamente anormales, Sangre (Barc), 24, 1057

Knuutila, 1980, Higher frequency of 5q− clone in bone marrow mitosis after culture than by a direct method, Scand J Haematol, 25, 358, 10.1111/j.1600-0609.1981.tb01414.x

Berger, 1980, Absence of chromosome abnormalities and acute leukemia: Relationship with normal bone marrow cells, CR Acad Sci Paris, 290, 1557

Vermaelen K, Michaux J-L, Louwagie A, Van Den Berghe H, (in press): Reciprocal translocation t(6;9)(p21;q33): A new characteristic chromosome anomaly in myeloid leukemias. Cancer Genet Cytogenet 10:125–131.

Schwartz S, Jiji R, Kerman S, Meekins J, Cohen MM, (in press): Translocation (6;9)(p23;q34) in acute nonlymphocytic leukemia. Cancer Genet Cytogenet 10:133–138.

Sandberg AA, Morgan R, McCallister JA, Kaiser-McCaw B, Hecht F, (in press): Acute myeloblastic leukemia (AML) with a t(6;9)(p23;q34): A specific subgroup of AML? Cancer Genet Cytogenet 10:139–142.

Berger, 1980, Cytogenetic studies on acute monocytic leukemia, Leukemia Res, 4, 119, 10.1016/0145-2126(80)90051-X

Hagemeijer, 1982, Translocation (9;11)(p21;q23) in three cases of acute monoblastic leukemia, Cancer Genet Cytogenet, 5, 95, 10.1016/0165-4608(82)90001-2

Nagasaka, 1983, Four cases of t(4;11) acute leukemia and its myelo-monocytic nature in infants, Blood, 61, 1174, 10.1182/blood.V61.6.1174.1174

Van Den Berghe, 1979, A new chromosome anomaly in acute lymphoblastic leukemia (ALL), Hum Genet, 46, 173, 10.1007/BF00291919

Arthur, 1983, Partial deletion of the long arm of chromosome 16 and bone marrow eosinophilia in acute nonlymphocytic leukemia: A new association, Blood, 61, 994, 10.1182/blood.V61.5.994.994

Yunis JJ (in press): Fragile sites and predisposition to leukemia and lymphoma. Cancer Genet Cytogenet (in press)