Frequency of NUP98-NSD1 fusion transcript in childhood acute myeloid leukaemia
- 14 August 2003
- journal article
- Published by Springer Science and Business Media LLC in Leukemia
- Vol. 17 (11), 2244-2247
- https://doi.org/10.1038/sj.leu.2403104
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Cryptic translocation t(5;11)(q35;p15.5) with involvement of the NSD1 and NUP98 genes without 5q deletion in childhood acute myeloid leukemiaGenes, Chromosomes and Cancer, 2002
- A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay.Blood, 2002
- NUP98 gene fusions in hematologic malignanciesLeukemia, 2001
- A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemiaBlood, 2001
- Standardized RT-PCR analysis of fusion gene transcripts from chromosome aberrations in acute leukemia for detection of minimal residual diseaseLeukemia, 1999
- The Importance of Diagnostic Cytogenetics on Outcome in AML: Analysis of 1,612 Patients Entered Into the MRC AML 10 TrialBlood, 1998
- The ABL-BCR fusion gene is expressed in chronic myeloid leukemiaBlood, 1993