Partial trisomy of chromosome 4 resulting from a novel t(4;7) translocation in a case of AML M2 with eosinophilia

Cancer Genetics and Cytogenetics

Volumn 86, Issue 1, 1996, Pages 89-91

  Hiorns, Lynne R ^a   Swansbury, G John ^a   Zomas, Athanassios ^a   Catovsky, Daniel ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; CASE REPORT; CHROMOSOME 4; CHROMOSOME 7; EOSINOPHILIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENE TRANSLOCATION; GENETICS; HUMAN; KARYOTYPING; LETTER; MALE; PRESCHOOL CHILD; TRISOMY;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 4; CHROMOSOMES, HUMAN, PAIR 7; EOSINOPHILIA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOCYTIC, ACUTE; MALE; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0029692334     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(95)00149-2     Document Type: Letter

References (14)

1. Mecucci C, Van Orshoven A, Tricot G, Michaux JL, Delannoy A, Van Den Berghe H (1986): Trisomy 4 identifies a subset of acute non lymphocytic leukemia (ANLL). Blood 67:1328-1332.
2. Zollino M, Leone G, Sica S, Bajer J, Neri G (1993): Trisomy 4 in acute myeloblastic and acute lymphoblastic leukemia. Cancer Genet Cytogenet 65:115-119.
3. Kwong YL, Ha SY, Liu HW, Chan LC (1993): Trisomy 4 may occur in a broad range of hematologic malignancies. Cancer Genet Cytogenet 69:139-140.
4. Keung YK, Kaplan B, Douer D (1994): Biphenotypic MO acute myeloid leukemia with trisomy 4. Leukemia and Lymphoma 14:181-184.
5. Sandberg A, Van Den Berghe H, Hecht F (1987): Trisomy 4 in hematologic disorders. Cancer Genet Cytogenet 26:175.
6. United Kingdom Cancer Cytogenetics Group (UKCCG) (1992): Primary, single, autosomal trisomies associated with hematological disorders. Leuk Res 16:841-851.
7. Norwrousion MR, Kubaschinski G, Pfeiffer R, Schaefer UW, Schmidt CG (1987): Identification of prognostic factors in adult patients with acute myeloid leukaemia (Meeting Abstract). 4th European Conference on Clinical Oncology and Cancer Nursing, Madrid, p. 177.
8. Vega RA, Flores L (1987): Early M1 bone marrow in Acute Myelogenous Leukaemia: a good prognostic factor (meeting abstract). Proc Annu Meet Am Assoc Cancer Res: 28:232.
9. Hiorns LR, Min T, Swansbury GJ, Zelent A, Dyer MJS, Catovsky D (1994): Interstitial insertion of retinoic acid receptor-a gene in acute promyelocytic leukemia with normal chromosomes 15 and 17. Blood 83:2946-2951.
10. Dauwerse JG, Kievits T, Beverstock GC, Van der Keur D, Smit E, Wessels HW, Hagemeijer A, Pearson PL, Van Ommen GJB, Breuning MH (1990): Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p. Cytogenet Cell Genet 53:126-128.
11. Keating MJ, Cork A, Broach Y, Smith T, Walters RS, McCredie KB, Trujillo J, Freireich EJ (1987): Toward a clinically relevant cytogenetic classification of acute myelogenous leukemia. Leuk Res 11:119-133.
12. Woods, WG, Nesbit ME, Buckley J, Lampkin BC, McCreadie S, Kim TH, Piomelli S, Kersey JH, Feig S, Bernstein I, Hammond D for the Children's Cancer Study Group (1985): Correlation of chromosome abnormalities with patient characteristics, histologic subtype, and induction success in children with acute nonlymphocytic leukemia. J Clin Oncol 3:3-11.
13. Ferrari S, Grande A, Zucchini P, Manfredini R, Tagliafico E, Rossi E, Temperani P, Torelli G, Emilia G, Torelli U (1993): Overexpression of c-kit in a leukemic cell population carrying a trisomy 4 and its relationship with the proliferative capacity. Leukemia Lymphoma 9:495-501.
14. Human Gene Mapping 11 (1991): Cytogenet Cell Genet 58:1-2200.