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Article

Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias.

Leukemia - 1 Apr 2004

Vandenberghe P, Wlodarska I, Michaux L, Zachée P, Boogaerts M, Vanstraelen D, Herregods M-C, Van Hoof A, Selleslag D, Roufosse F, Maerevoet M, Verhoef G, Cools J, Gilliland D G, Hagemeijer A, Marynen P

Abstract excerpt

Detection of the FIP1L1-PDGFRA fusion gene or the corresponding cryptic 4q12 deletion supports the diagnosis of chronic eosinophilic leukemia (CEL) in patients with chronic hypereosinophilia. We retrospectively characterized 17 patients fulfilling WHO criteria for idiopathic hypereosinophilic syn...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 14973504
DOI: 10.1038/sj.leu.2403313

Genes

CEL
PDGFRA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14973504-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias.PMID 14973504Read ↗

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