Objective: To establish the method of aneuploidy detection in human oocytes by multicolor fluorescence in-situ hybridization (M-FISH).
目的建立多色荧光原位杂交技术检测人卵细胞染色体非整倍体的方法。
Transpositional points between chromosome 6 and 12 were anchored in 1 and 3 BAC clone's pool respectively by fluorescence in situ hybridization technology of pachytene chromosomes.
通过粗线期染色体荧光原位杂交技术，将发生易位的第6号和第12号染色体的易位点分别锚定在1个和3个BAC克隆库中。
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。
Modern molecular biotechnology such as fluorescence in situ hybridization and DNA fingerprinting was widely applied in wastewater treatment.
荧光原位杂交、DNA指纹等现代分子生物技术在废水治理过程中得到了广泛的应用。
The basic techniques currently used involve embryo biopsy, the polymerase chain reaction and fluorescence in situ hybridization.
其技术主要包括胚胎活检、聚合酶链反应及荧光原位杂交。
Objective To investigate the value of multiplex fluorescence in situ hybridization (M-FISH) in the detection of complex chromosomal abnormalities (CCAs) of chronic lymphocytic leukemia (CLL).
目的探讨多重荧光原位杂交(M -FISH)技术检测慢性淋巴细胞白血病(CLL)复杂核型异常(CCA)的价值。
BAC clones corresponding to telomeres, as well as to the centromere position and the gap sizes between contigs, were determined by BAC-pachytene chromosome fluorescence in situ hybridization (FISH).
端粒克隆、着丝粒克隆以及重叠群之间空缺的大小都经过粗线期染色体荧光原位杂交鉴定。
All 3 ESS were found to harbor ZC3H7B-BCOR gene fusions by targeted sequencing and fluorescence in situ hybridization.
通过靶向测序和荧光原位杂交技术发现，3例均存在ZC 3h7b -BCOR基因融合。
Detection of chromosomal abnormalities by fluorescence in situ hybridization (FISH) analysis has not been well-studied in FNA samples of pancreatic masses.
目前我们采用荧光原位杂交(FISH)分析法对胰腺肿块细针穿刺活检(FNA)样本行染色体异常检测还没有深入研究。
The remaining case demonstrated SS18 rearrangement by fluorescence in situ hybridization.
用荧光免疫杂交的方法，发现其他病例均发生SS18基因的重排。
All 5 cases exhibited at least focal classic histologic findings. All harbored DDIT3 gene rearrangements, and none harbored MDM2 amplifications according to fluorescence in situ hybridization.
这5例至少局灶存在经典的组织学形态，荧光原位杂交检测DDIT3基因均出现重排，无mdm2扩增。
Objective To study the numerical abnormality of chromosomes in lung cancer by dual-color fluorescence in situ hybridization(FISH).
目的探讨一种以胎盘绒毛取样进行荧光原位杂交（FISH）快速诊断染色体数目的方法。
In addition, the technique of hybridization in situ with fluorescence allowed him to identify new recurrent genetic changes that are involved in the appearance of this pathology.
另外，荧光原位杂交技术可以鉴别有关病理学表现的新的循环遗传改变。
Methods:Multicolor fluorescence in situ hybridization (M-FISH) was applied to check the chromosome status in oocytes for chromome 13,16,18,21 and 22.
方法：取试管婴儿助孕技术后未能受精成功的卵细胞，采用多色荧光原位杂交方法检测卵细胞13，16 ，18，2 1和2 2号染色体的情况。
Methods:Multicolor fluorescence in situ hybridization (M-FISH) was applied to check the chromosome status in oocytes for chromome 13,16,18,21 and 22.
方法：取试管婴儿助孕技术后未能受精成功的卵细胞，采用多色荧光原位杂交方法检测卵细胞13，16 ，18，2 1和2 2号染色体的情况。
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