Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in aNUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia

This publication has 14 references indexed in Scilit:

• Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts
  Genes, Chromosomes and Cancer, 2004
• Analysis of translocations that involve the NUP98 gene in patients with 11p15 chromosomal rearrangements
  Genes, Chromosomes and Cancer, 2004
• Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemia
  British Journal of Haematology, 2004
• Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions
  Genes, Chromosomes and Cancer, 2003
• Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Francais de Cytogenetique Hematologique (GFCH)
  Blood, 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 malignancies
  Leukemia, 2001
• A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia
  Blood, 2001
• An Optimized Set of Human Telomere Clones for Studying Telomere Integrity and Architecture
  American Journal of Human Genetics, 2000
• Variant and Masked Translocations in Acute Promyelocytic Leukemia
  Leukemia & Lymphoma, 1996