A myeloproliferative disease in two infants associated with eosinophilia and chromosome t(1;5) translocation
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1987.tb01331.x/fullpdf
Reference16 articles.
1. Associated abnormalities of chromosomes 1, 5, and 11 in dysmyelopoietic syndromes
2. Distinct haematological disorder with deletion of long arm of No. 5 chromosome
3. Clinical characteristics and prognosis of 50 patients with a myeloproliferative syndrome and deletion of part of the long arm of chromosome 5
4. Chromosomal localization of the human c-fmsoncogene
5. A unique pattern of central nervous system leukemia in acute myelomonocytic leukemia associated with inv(16)(p13q22)
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2. Myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase fusion genes: A workshop report with focus on novel entities and a literature review including paediatric cases;Histopathology;2023-08-08
3. Myeloproliferative neoplasm with eosinophilia and PDGFR beta rearrangement in an infant;Pediatric Blood & Cancer;2022-06-27
4. A report of an unusual case of pediatric eosinophilia associated with platelet-derived growth factor receptor-beta rearrangement;Indian Journal of Medical and Paediatric Oncology;2020-09
5. A Rare Case of Extramedullary T/Myeloid Mixed Phenotype Acute Leukemia with t(1;5)(q23;q33);Case Reports in Pathology;2016
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