Interstitial Deletion of the Short Arm of Chromosome 12 during Clonal Evolution in Myelodysplastic Syndrome with t(5;12)(q13;p13) Involving the ETV6 Gene
- 1 June 2000
- journal article
- case report
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 119 (2) , 113-117
- https://doi.org/10.1016/s0165-4608(99)00227-7
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: a combined PCR and Southern blotting analysisLeukemia, 1998
- Establishment of a novel human acute myeloblastic leukemia cell line (YNH-1) with t(16;21), t(1;16) and 12q13 translocationsLeukemia, 1997
- Genomic organization of TEL: the human ETS-variant gene 6.Genome Research, 1996
- The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignanciesCytogenetic and Genome Research, 1996
- ETV6Gene Rearrangements in Hematopoietic Malignant DisordersLeukemia & Lymphoma, 1996
- Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2Blood, 1996
- Identification of cytogenetically undetected 12p13 translocations and associated deletions with fluorescence in situ hybridizationGenes, Chromosomes and Cancer, 1995
- Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocationCell, 1994
- Translocations involving 12p in acute myeloid leukemia: Association with prior myelodysplasia and exposure to mutagenic agentsGenes, Chromosomes and Cancer, 1992
- Cytogenetic study of 105 children with acute lymphoblastic leukemiaEuropean Journal of Haematology, 1988