Eosinophilic leukaemia with an abnormality of 5q31, the site of the IL-5 gene
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2257.1991.tb00271.x/fullpdf
Reference15 articles.
1. A myeloproliferative disease in two infants associated with eosinophilia and chromosome t(l;5) translocation;Darbyshire;Br. J. Haemat.,1987
2. Evidence for the clonal nature of hypereosinophilic syndrome;Silva;Cancer Genet. Cytogenet.,1988
3. 8;21 chromosome translocation in eosinophilic leukaemia;Kaneko;Cancer Genet. Cytogenet.,1983
4. Abnormalities of chromosome 12p13 and malignant proliferation of eosinophils: a nonrandom association;Keene;Br. J. Haemat.,1987
5. Mutations of the Kirsten-ras proto-oncogene in human preleukaemia;Liu;Nature,1987
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2. Chronic basophilic leukemia: a rare form of chronic myeloproliferative neoplasm;Human Pathology;2009-08
3. Myelodysplastic syndrome accompanied by basophilia and eosinophilia with t(5;12)(q31;p13);Cancer Genetics and Cytogenetics;2007-10
4. Receptor tyrosine kinase mutations in myeloid neoplasms;British Journal of Haematology;2002-05-19
5. 21q22 balanced chromosome aberrations in therapy-related hematopoietic disorders: Report from an International Workshop;Genes, Chromosomes and Cancer;2002-03-12
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