NUP98-NSD1fusion in association withFLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR-Reference-Cited by-同舟云学术

NUP98-NSD1fusion in association withFLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR

Published:2013-09-02 Issue:11 Volume:52 Page:1053-1064
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Akiki Susanna¹²,Dyer Sara A.¹²,Grimwade David³,Ivey Adam³⁴,Abou-Zeid Nervana¹,Borrow Julian¹²,Jeffries Sally¹,Caddick Judith¹,Newell Hayley¹,Begum Suriya¹,Tawana Kiran⁵,Mason Joanne¹,Velangi Mark⁵,Griffiths Michael¹²

Affiliation:

1. West Midlands Regional Genetics Laboratory, Birmingham Women's NHS foundation Trust; Birmingham UK

2. School of Cancer Sciences; College of Medical and Dental Sciences, University of Birmingham; Birmingham UK

3. Department of Medical and Molecular Genetics, King's College London School of Medicine; London UK

4. Molecular Oncology Diagnostics Unit; GSTS Pathology; London UK

5. Haematology Department; Birmingham Children's Hospital; Birmingham UK

Publisher

Wiley

Subject

Cancer Research,Genetics

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4. 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;Brown;Blood,2002

5. Frequency of NUP98/NSD1 fusion transcript in childhood acute myeloid leukaemia;Cerveira;Leukemia,2003

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