研究人员特定地寻找染色体数发生易位的数量染色体易位（Chromosome translocations）是与电离辐射暴露相关的DNA损伤累积的一个可靠指标，这是因为它不能够像其它染色体异常一样快速地从血液中清除。
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chromosome translocation t 染色体易位t
chromosome translocation lines 染色体易位系
chromosome translocation carrier 染色体易位携带者
complex chromosome translocation 复合型染色体易位
recurrent chromosome translocation 重现染色体易位
spontaneous chromosome translocation 自发易位
wheat-rye chromosome translocation 小麦
A few of chromosome bridges,laggard chromosomes micronucleus and nonsynchronous division are found in some PMCs at anaphaseⅠandⅡ,telophaseⅠandⅡ. It suggests that chromosome translocation or inversion has occurred.
部分PMCs后期Ⅰ、后期Ⅱ和末期Ⅰ、末期Ⅱ发现有染色体桥、落后染色体、微核及不同步分裂等减数分裂异常现象,表明染色体组中可能存在易位或倒位等结构变异。
参考来源 - 菊亚族六个种的细胞学及太行菊的生殖生物学研究·2,447,543篇论文数据，部分数据来源于NoteExpress
Using genomic PCR and sequencing, FLT3/ITD mutation with or without chromosome translocation were examined in AML patients.
采用PCR联合序列检测伴有或不伴有染色体易位的急性髓性白血病患者FLT3基因突变情况。
The variance component of cross and backcross generations of quantitative character controlled by multigenes is studied on condition of chromosome translocation.
研究了染色体易位情况下，多基因控制的数量性状杂交及回交世代的方差组成。
This study was aimed to explore the relationship of 6; 9 chromosome translocation with DEK-CAN fusion gene expression in patients with acute myeloid leukemia (AML) and its clinical significance.
本研究旨在探讨急性髓系白血病(aml)患者6；9染色体易位与DEK - CAN融合基因表达之间的关系及临床意义。
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