1·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。
2·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。
3·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。
4·Moreover, exogenous agents, such as ionizing radiation and some chemicals can result in chromosome translocation and tumorigenesis because of their role on induction of DNA double strand breaks.
此外，外界因素，如电离辐射和某些化学药物等因素使DNA双链断裂，也可能导致染色体转位和癌变。
5·Otherwise, the chromosome break and rearrangement induced by radiation maybe play important pole in leading to the translocation and misalignment of cancer genes and other correlated genes.
另外，辐射所致染色体的断裂和重排对癌基因和其他相关基因的移位和失调可能起着重要作用。
6·A reciprocal translocation between 6 and 11 was further confirmed by chromosome painting technique in 5 cases.
全染色体涂染技术分析也证实5例患者6号和11号染色体之间发生了相互易位。
7·Objective To explore the differences between radiation-induced translocation and dicentric chromosome aberrations detected by multicolor fluorescence in situ hybridization (M-FISH) method.
目的探讨用多色荧光原位杂交(M FISH)技术检测的易位和双着丝粒染色体畸变的差异。
8·Said disease-resisting translocation line Y96060 can be confirmed by means of cytogenetic analysis, chromosome C zoning and in situ hybridization and RAPD technique.
抗病易位系Y96060可通过细胞遗传分析，染色体C分带和原位杂交技术，RAPD技术得到确认。