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Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myeloma
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Molecular characterization of the idiopathic hypereosinophilic syndrome (HES) in 35 French patients with normal conventional cytogenetics
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NUP98 rearrangements in hematopoietic malignancies : a study of the Groupe francophone de cytogénétique hématologique
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High occurrence of JAK2 V617 mutation in refractory anemia with ringed sideroblasts associated with marked thrombocytosis
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Hypereosinophilia with abnormal T cells, trisomy 7 and elevated TARC serum level
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Disruption and aberrant expression of HMGA2 as a consequence of diverse chromosomal translocations in myeloid malignancies
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Evaluation of minimal residual disease by interphase FISH in multiple myeloma : does complete remission exist ?
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Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome
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Investigation of minimal residual disease in adult Ph1 positive acute lymphoblastic leukemia by a combination of cell sorting and fluorescence in situ hybridization : A preliminary study on 6 cases
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Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis
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Published in Leukemia (01.04.1992)
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Published in Leukemia (01.04.1992)
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De novo myelodysplastic syndrome (MDS) with deletion of the long arm of chromosome 20: A subtype of MDS with distinct hematological and prognostic features?
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Coexistence of AML1 RUNX1 and BCR-ABL point mutations in an imatinib-resistant form of CML
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Nonrandom 4p13 rearrangements of the RhoH/TTF gene, encoding a GTP-binding protein, in non-Hodgkin's lymphoma and multiple myeloma
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