Fluorescencein situhybridization characterization of ider(20q) in myelodysplastic syndrome
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2008.07436.x/fullpdf
Reference11 articles.
1. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions;Douet-Guilbert;Annals of Hematology,2008
2. Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-);Li;British Journal of Haematology,2004
3. FISH studies identify the i(20q-) anomaly as a der(20)del(20)(q11q13)idic(20)(p11);Li;Genes, Chromosomes and Cancer,2006
4. Isodicentric 20q- in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2);Li;Cancer Genetics and Cytogenetics,2008
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4. Expression analysis of genes located within the common deleted region of del(20q) in patients with myelodysplastic syndromes;Leukemia Research;2019-09
5. ASXL1 gene alterations in patients with isolated 20q deletion;Neoplasma;2019
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