Translocation t(3;17)(q26;q22): A marker of acute disease in myeloproliferative disorders?
- 1 June 1984
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 12 (2) , 111-119
- https://doi.org/10.1016/0165-4608(84)90122-5
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Analysis of the breakpoints in translocation (15;17) Observed in 4 patients with acute promyelocytic leukemiaHuman Genetics, 1982
- Abnormalities of chromosome No. 17 in myeloproliferative disordersCancer Genetics and Cytogenetics, 1982
- Correlations between the clinical course, characteristics of blast cells, and karyotype patterns in chronic myeloid leukemiaHuman Genetics, 1981
- Acute nonlymphocytic leukemia, preleukemia, and acute myeloproliferative syndrome secondary to treatment of other malignant diseases. Clinical and cytogenetic characteristics and results of in vitro culture of bone marrow and HLA typingBlood, 1981
- PARTICULAR SECONDARY CHROMOSOME CHANGES IN CHRONIC LEUKEMIA-T(8-17) - REPORT OF 2 CASES1981
- C‐Group Chromosome Abnormalities in Bone Marrow Cells of Three Children with Dyshaematopoiesis of Unknown OriginBritish Journal of Haematology, 1980
- The chromosomes and causation of human cancer and leukemia: XXXVIII. Cytogenetic experience in Ph1‐negative chronic myelocytic leukemia (CML)American Journal of Hematology, 1979
- Patial trisomy 1 due to 1/17 translocation in Ph'-Positive chronic myelocytic leukemiaHuman Genetics, 1979
- Chromosome abnormalities and clinical and morphologic manifestations of chronic myeloid leukemiaHuman Genetics, 1978