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Characterization of 5q deletions by subtelomeric probes and spectral karyotyping.

作者信息

Ning Y, Liang J C, Nagarajan L, Schröck E, Ried T

机构信息

Genome Technology Branch, National Human Genome Research Institute, Bethesda, Maryland, USA.

出版信息

Cancer Genet Cytogenet. 1998 Jun;103(2):170-2. doi: 10.1016/s0165-4608(97)00417-2.

DOI:10.1016/s0165-4608(97)00417-2
PMID:9614919
Abstract
摘要

相似文献

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Characterization of 5q deletions by subtelomeric probes and spectral karyotyping.
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Cytogenetic, spectral karyotyping, fluorescence in situ hybridization, and comparative genomic hybridization characterization of two new secondary leukemia cell lines with 5q deletions, and MYC and MLL amplification.两个具有5q缺失、MYC和MLL扩增的新的继发性白血病细胞系的细胞遗传学、光谱核型分析、荧光原位杂交及比较基因组杂交特征
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Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping.运用光谱核型分析对五例急性髓系白血病患者进行核型优化
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A half cryptic derivative der(18)t(5;18)pat identified by M-FISH and subtelomere probes: clinical findings and review of subtelomeric rearrangements.通过M-FISH和亚端粒探针鉴定出的一个半隐匿性衍生染色体der(18)t(5;18)pat：临床发现及亚端粒重排综述
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Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation.5号染色体q臂缺失及髓系细胞转化过程中α-连环蛋白（CTNNA1）编码基因的表观遗传抑制
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Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions.对髓系疾病患者复杂核型中5号染色体畸变的评估揭示了它们对双着丝粒和三着丝粒染色体的影响，导致关键5q区域的缺失。
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