A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia

Cancer Genetics and Cytogenetics

Volumn 119, Issue 1, 2000, Pages 77-79

  Brückner, Roland ^a   Jentsch Ullrich, Kathleen ^a   Franke, Astrid ^a   Wieacker, Peter ^a   Stumm, Markus ^a  

^a UNIVERSITY HOSPITAL MAGDEBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE MYELOMONOCYTIC LEUKEMIA; ADULT; ARTICLE; CASE REPORT; CHROMOSOME TRANSLOCATION; CYTOGENETICS; DISEASE COURSE; HUMAN; LEUKEMOGENESIS; PRIORITY JOURNAL;

CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 19; HUMANS; IMMUNOPHENOTYPING; KARYOTYPING; LEUKEMIA, MYELOMONOCYTIC, ACUTE; MALE; MIDDLE AGED; TRANSLOCATION, GENETIC;

EID: 17644433356     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00214-9     Document Type: Article

References (6)

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3. Mark H.F.L., Gray J., Rintels P. Translocation 2;19 in a patient with a probable relapsed acute myeloid leukemia. Pathobiology. 65:1997;223-228.
4. Soenen V., Preudhomme C., Roumier C., Daudignon A., Lai J.L., Fenaux P. 17p deletion in acute myeloid leukemia and myelodyspastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ. Blood. 91:1998;1008-1015.
5. Sterkers Y., Preudhomme C., Lai J.L., Demory J.L., Caulier M.T., Wattel E., Bordessoule D., Bauters F., Fenaux P. Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea. high proportion of cases with 17p deletion Blood. 91:1998;616-622.
6. Sankar M., Tanaka K., Kumaravel T.S., Arif M., Shintani T., Yagi S., Kyo T., Dohy H., Kamada N. Identification of a commonly deleted region at 17p13.3 in leukemia and lymphoma associated with 17p abnormality. Leukemia. 12:1998;510-516.