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首页> 外文期刊>Advances in hematology >Complex Variant t(9;22) Chromosome Translocations in Five Cases of Chronic Myeloid Leukemia
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Complex Variant t(9;22) Chromosome Translocations in Five Cases of Chronic Myeloid Leukemia

机译:5例慢性粒细胞白血病的复杂变体t(9; 22)染色体易位

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摘要

The Philadelphia (Ph1) chromosome arising from the reciprocal t(9;22) translocation is found in more than 90% of chronic myeloid leukemia (CML) patients and results in the formation of the chimeric fusion geneBCR-ABL. However, a small proportion of patients with CML have simple or complex variants of this translocation, involving various breakpoints in addition to 9q34 and 22q11. We report five CML cases carrying variant Ph translocations involving both chromosomes 9 and 22 as well as chromosomes 3, 5, 7, 8, or 10. G-banding showed a reciprocal three-way translocation involving 3q21, 5q31, 7q32, 8q24, and 10q22 bands.BCR-ABLfusion signal on der(22) was found in all of the cases by FISH.
机译:在90%以上的慢性粒细胞白血病(CML)患者中发现了由相互的t(9; 22)易位引起的费城(Ph1)染色体,并导致嵌合融合基因BCR-ABL的形成。但是,一小部分CML患者具有这种易位的简单或复杂变体,除了9q34和22q11之外还涉及各种断点。我们报告了五例CML病例,它们携带涉及染色体9和22以及染色体3、5、7、8或10的变异Ph易位。G谱带显示了涉及3q21、5q31、7q32、8q24和3q的双向三向易位。通过FISH在所有病例中都发现der(22)上有10q22条带的BCR-ABLfusion信号。

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