Hidden chromosomal aberrations are rare in primary myelodysplastic syndromes with evolution to acute myeloid leukaemia and normal cytogenetics
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology,Hematology
Reference26 articles.
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1. Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?;Leukemia Research;2012-07
2. Apport de l’hybridation in situ en fluorescence (FISH) pour la détection des anomalies cytogénétiques dans les syndromes myélodysplasiques;Revue Francophone des Laboratoires;2011-06
3. Cytogenetics of MDS;The Myelodysplastic Syndromes;2011
4. Diagnostic Tools in the Indications for Allogeneic Stem Cell Transplantation in Myelodysplastic Syndromes;Biology of Blood and Marrow Transplantation;2010-01
5. Comparison of I-FISH and G-banding for the detection of chromosomal abnormalities during the evolution of myelodysplastic syndrome;Brazilian Journal of Medical and Biological Research;2009-11
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