Characterization of a Highly Complex Region in Xq13 and Mapping of Three Isodicentric Breakpoints Associated with Preleukemia
- 15 March 2000
- Vol. 64 (3) , 221-229
- https://doi.org/10.1006/geno.2000.6128
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A)Human Molecular Genetics, 1999
- Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literatureBritish Journal of Haematology, 1995
- Cytogenetic and FISH studies of abnormal X chromosomes in a patient with ANLLCancer Genetics and Cytogenetics, 1992
- Differential distribution of long and short interspersed element sequences in the mouse genome: chromosome karyotyping by fluorescence in situ hybridization.Proceedings of the National Academy of Sciences, 1990
- Twenty-six patients with hematologic disorders and X chromosome abnormalitiesCancer Genetics and Cytogenetics, 1989
- Human mRNA polyadenylate binding protein: evolutionary conservation of a nucleic acid binding motifNucleic Acids Research, 1987
- Chromosome Abnormalities in Malignant Hematologic DisordersMayo Clinic Proceedings, 1985
- Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomalNature, 1985
- 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