Cytogenetic abnormalities in pediatric myelodysplastic syndrome: A report of three cases
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference33 articles.
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2. Proposals for the classification of the myelodysplastic syndromes;Bennett;Br J Hematol,1982
3. Myelodysplasia;Chessells;Bailliére's Clin Hematol,1991
4. Experience in pediatric myelodysplastic syndromes;Gadner;Hematol Oncol Clin North Am,1992
5. Myelodysplastic syndromes in childhood—classification, epidemiology and treatment;Hasle;Leukemia Lymphoma,1994
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1. Myelodysplastic syndromes with isolated deletion of the long arm of the chromosome X as a sole cytogenetic change;Cancer Genetics and Cytogenetics;2006-05
2. The effectiveness of high–resolution-comparative genomic hybridization in detecting the most common chromosomal abnormalities in pediatric myelodysplastic syndromes;Cancer Genetics and Cytogenetics;2005-04
3. Monosomy 21 in hematologic diseases;Cancer Genetics and Cytogenetics;2003-04
4. Characterization of additional genetic events in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion: a molecular cytogenetics study;Leukemia;2001-09
5. Paediatric myelodysplastic syndrome (MDS) and juvenile chronic myelogenous leukaemia (JCML) detected by cytogenetic and FISH techniques;Clinical & Laboratory Haematology;1999-12
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