Molecular cytogenetic analysis of monosomy 7 in pediatric patients with myelodysplastic syndrome
Author:
Publisher
Wiley
Subject
Hematology
Reference16 articles.
1. Biology and pathogenesis of the myelodysplastic syndromes;List;Semin Oncol,1992
2. Childhood monosomy revisited;Evans;Br J Hematol,1987
3. Monosomy 7 in childhood: A myeloproliferative disorder;Seiff;Br J Hematol,1981
4. Interphase cytogenetics;Herrington;Neurochem Res,1990
5. Rapid interphase and metaphase assessment of specific chromosomal changes in neuroectodermal tumour cells by in situ hybridization with chemically modified DNA probes;Cremer;Exp Cell Res,1988
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1. Molecularly Targeted Therapies in Pediatric Myelodysplastic Syndromes;Molecularly Targeted Therapy for Childhood Cancer;2010
2. Fluorescence in situ Hybridization Reveals Closely Correlated Results in Cytological and Histological Specimens of Hematological Neoplasias Compared to Conventional Cytogenetics;Pathobiology;2006
3. Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses.;Cancer Genetics and Cytogenetics;2001-02
4. Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasia;British Journal of Haematology;2000-09
5. Discrepant Cytogenetic and Fluorescence In Situ Hybridization Results in a 26-Year-Old Male with Early T-Cell Acute Lymphocytic Leukemia;Cancer Genetics and Cytogenetics;1998-10
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