A novel isoderivative chromosome 20 in a patient with chronic myelomonocytic leukemia
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference11 articles.
1. Deletion of the long arm of chromosome 20 [del(20)(q11)] in myeloid disorders;Testa;Blood,1978
2. Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q−);Li;Br J Haematol,2004
3. Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes;Saunders;Cancer Genet Cytogenet,2005
4. Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies;Ligon;Cancer Genet Cytogenet,2005
5. A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies;MacKinnon;Cancer Genet Cytogenet,2005
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. L’association des neutrophiles hypogranulaires et vacuolisés à l’érythrophagocytose par les neutrophiles est un marqueur utile dans les syndromes myélodysplasiques avec del(20q) ou ider(20q) : une étude multicentrique;Immuno-analyse & Biologie Spécialisée;2012-02
2. Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study;Annals of Hematology;2011-07-09
3. Pulmonary Alveolar Proteinosis as a Terminal Complication in a Case of Myelodysplastic Syndrome with idic(20q–);Acta Haematologica;2010
4. Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH;Annals of Hematology;2009-05-15
5. Fluorescencein situhybridization characterization of ider(20q) in myelodysplastic syndrome;British Journal of Haematology;2008-12
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