Cryptic chromosomal aberrations waiting to be discovered-Reference-Cited by-同舟云学术

Cryptic chromosomal aberrations waiting to be discovered

Published:2005-12-15 Issue:2 Volume:20 Page:210-211
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Lahortiga I,Cools J

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/2404078.pdf

Reference21 articles.

1. Paulsson K, Békássy AN, Olofsson T, Mitelman F, Johansson B, Panagopoulos I . A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin specific protease gene USP42. Leukemia 2006; 20: 224–229.

2. Golub TR, Barker GF, Bohlander SK, Hiebert SW, Ward DC, Bray-Ward P et al. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc Natl Acad Sci USA 1995; 92: 4917–4921.

3. De Keersmaecker K, Marynen P, Cools J . Genetic insights in the pathogenesis of T-cell acute lymphoblastic leukemia. Haematologica 2005; 90: 1116–1127.

4. Cools J, Stover EH, Wlodarska I, Marynen P, Gilliland DG . The FIP1L1-PDGFRalpha kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia. Curr Opin Hematol 2004; 11: 51–57.

5. Ishkanian AS, Malloff CA, Watson SK, DeLeeuw RJ, Chi B, Coe BP et al. A tiling resolution DNA microarray with complete coverage of the human genome. Nat Genet 2004; 36: 299–303.

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