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Microarray-based comparative genomic hybridisation reveals additional recurrent aberrations in adult patients evaluated for myelodysplastic syndrome with normal karyotype.

作者信息

Ouahchi Ines, Zhang Luduo, Benitez Brito Ramon, Benz Rudolf, Müller Rouven, Bonadies Nicolas, Tchinda Joëlle

机构信息

Department of Cytogenetics, Molecular Genetics and Reproductive Biology, Farhat Hached University Hospital, Sousse, Tunisia.

Department of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.

出版信息

Br J Haematol. 2019 Jan;184(2):282-287. doi: 10.1111/bjh.15068. Epub 2018 Jan 9.

DOI:10.1111/bjh.15068
PMID:29318588
Abstract
摘要

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Microarray-based comparative genomic hybridisation reveals additional recurrent aberrations in adult patients evaluated for myelodysplastic syndrome with normal karyotype.基于微阵列的比较基因组杂交技术揭示了在接受核型正常的骨髓增生异常综合征评估的成年患者中存在其他复发性畸变。
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Array comparative genomic hybridization of peripheral blood granulocytes of patients with myelodysplastic syndrome detects karyotypic abnormalities.Array 比较基因组杂交技术检测骨髓增生异常综合征患者外周血粒细胞的核型异常。
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Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.17号染色体短臂拷贝数中性杂合性缺失及TP53基因纯合突变与新诊断的骨髓增生异常综合征患者的复杂染色体畸变相关。
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Identify latent chromosomal aberrations relevant to myelodysplastic syndromes.鉴定与骨髓增生异常综合征相关的潜在染色体异常。
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Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance.正常核型骨髓增生异常综合征的全面阵列 CGH 揭示了具有预后相关性的隐藏的反复和个体基因组拷贝数改变。
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High-resolution genomic arrays facilitate detection of novel cryptic chromosomal lesions in myelodysplastic syndromes.高分辨率基因组阵列有助于检测骨髓增生异常综合征中新发的隐匿性染色体病变。
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