Isochromosome 17 in a Patient with a Myeloproliferative Disorder Terminating in Eosinophilic Leukemia
Author:
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0954-6820.1979.tb13519.x/fullpdf
Reference28 articles.
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3. Eosinophilic leukemia. Report of five cases and review of literature;Benvenisti;Ann Intern Med,1969
4. Chromosomal aneuploidy in a patient with hypereosinophilic syndrome. Evidence for a malignant disease;Bitran;Am J Med,1977
5. Different composition of the eosinophilic bone marrow pool in reactive eosino-philia and eosinophilic leukaemia;Brandt;Acta Med Scand,1977
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1. Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53;Cancer;2011-10-28
2. Molecular Classification and Pathogenesis of Eosinophilic Disorders: 2005 Update;Acta Haematologica;2005
3. Cytogenetic and molecular genetic aspects of eosinophilic leukaemias;British Journal of Haematology;2003-07
4. Hypereosinophilia Progressing to Granulocytic Sarcoma and Acute Myelocytic Leukemia with Trisomy 8: A Case Report and Review of the Literature;Hematology;1999-01
5. Chronic Eosinophilic Leukemia and Hypereosinophilic Syndromes;Cancer Genetics and Cytogenetics;1998-12
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