Isodicentric X chromosomes involving the Xq13 breakpoint in myelodysplasia and acute nonlymphocytic leukemia
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 30 (1) , 43-52
- https://doi.org/10.1016/0165-4608(88)90091-x
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Chromosome instability is associated with hypodiploid clones in myelodysplastic syndromesHereditas, 2008
- Translocation X;10 in a case of congenital acute monocytic leukemiaCancer Genetics and Cytogenetics, 1985
- Translocation 1;19—A new cytogenetic abnormality in acute lymphocytic leukemiaCancer Genetics and Cytogenetics, 1984
- Complete or partial trisomy for the long arm of chromosome 1 in patients with various hematologic malignanciesHuman Genetics, 1983
- Fluorodeoxyuridine synchronization of bone marrow culturesCancer Genetics and Cytogenetics, 1983
- On the Xq13 Breakpoint: Clinical and Cytogenetic Observations in a Patient with Acute Myelogenous LeukemiaActa Haematologica, 1983
- Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?Cancer Genetics and Cytogenetics, 1982
- Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemiaBlood, 1982
- Cytogenetic follow-up of patients with nonlymphocytic leukemia. II. Acute nonlymphocytic leukemiaCancer Genetics and Cytogenetics, 1981
- Chromosomal banding patterns in 88 cases of acute nonlymphocytic leukemiaLeukemia Research, 1978