Article révisé par les pairs
Titre:
  • A case of FIP1L1-PDGFRA-positive chronic eosinophilic leukemia with a rare FIP1L1 breakpoint.
Auteur:Lambert, Frédéric; Heimann, Pierre; Herens, C.; Chariot, Alain; Bours, Vincent
Informations sur la publication:The Journal of molecular diagnostics, 9, 3, page (414-419)
Statut de publication:Publié, 2007-07
Sujet CREF:Cancérologie
MeSH keywords:Adult
Amino Acid Sequence
Base Sequence
Chromosome Breakage
Chromosomes, Human, Pair 4
Chronic Disease
DNA Mutational Analysis
Humans
Hypereosinophilic Syndrome -- diagnosis -- genetics
In Situ Hybridization, Fluorescence
Male
Molecular Sequence Data
Mutant Chimeric Proteins -- genetics
Polymerase Chain Reaction -- methods
Receptor, Platelet-Derived Growth Factor alpha -- genetics
Translocation, Genetic
mRNA Cleavage and Polyadenylation Factors -- genetics
Note générale:Case Reports
Journal Article
SCOPUS: ar.j
Langue:Anglais
Identificateurs:urn:issn:1525-1578
info:doi/10.2353/jmoldx.2007.060196
info:pii/S1525-1578(10)60411-4
info:scp/34548148179
info:pmid/17591942
PMC1899422