1) two-color fluorescence in situ hybridization
双色荧光原位杂交
1.
Detection of numerical aberrations of chromosomes 7 and 8 in sperms of workers exposed to benzene series by two-color fluorescence in situ hybridization;
双色荧光原位杂交检测苯系物接触者精子7、8号染色体数目畸变
2) 22q11.2 deletion
双色细菌人工染色体-荧光原位杂交
3) DD-FISH
间期双色双融合荧光原位杂交
4) triple-color fluorescence in situ hybridization
三色荧光原位杂交
1.
Objective: To analyze the numerical aberration of chromosome X, Y and 18 in the spermatozoa of asthenospermia patients by triple-color fluorescence in situ hybridization.
目的:利用三色荧光原位杂交方法分析弱精子症患者精子X,Y,18号染色体数目畸变。
5) Multicolor fluorescence in situ hybridization
多色荧光原位杂交
1.
The clinical application of multicolor fluorescence in situ hybridization;
多色荧光原位杂交技术的临床应用
2.
Methods A complex chromosomal rearrangement (CCR) invol ved in chromosomes 5, 16 and 20 in a 29-year-old male carrier was determined b y chro mosomal microdissection and multicolor fluorescence in situ hybridization(M -FIS H), and family degree investigation was further performed.
方法对1例涉及5号、16号和20号染色体复杂重排核型的男性携带者,应用多色荧光原位杂交和显微切割技术进一步分析确定其核型,并进行家系调查。
3.
We elaborated a 47, XY, inv(9)(p11q13), +mar and a 46,XY,t(5;?) by combining a range of cytogenetic techniques, including multicolor fluorescence in situ hybridization (M-FISH), G-banding and NOR.
用多色荧光原位杂交技术结合G显带技术和NOR技术,对1例47,XY,inv(9)(p11q13),+mar和1例46,XY,t(5;?)核型进行诊断。
6) multicolor FISH
多色荧光原位杂交
1.
BACKGROUND & AIM: To investigate the difference of bone marrow chromosome aberrations induced by acute or chronic ionizing radiation with multicolor FISH (M-FISH) method.
背景与目的:探索多色荧光原位杂交(Multicolorfluorescenceinsituhybridization,M-FISH)技术分析急慢性电离辐射照射诱发的小鼠染色体畸变的差异。
2.
In this study, multicolor FISH analysis on metaphase chromosomes of spinach with biotin-labeled 25S rDNA, DIG-labeled telomere sequences and biotin-labeled and DIG-labeled 5S rDNA was performed.
以拟南芥25S rDNA、5S rDNA以及端粒序列为探针对菠菜的中期染色体进行了多色荧光原位杂交分析,其中25S rDNA用生物素标记,端粒序列用地高辛标记,5S rDNA用生物素和地高辛共同标记。
补充资料:荧光原位杂交
荧光原位杂交
是以荧光素标记取代核素标记而形成的一种新的原位杂交方法。利用已知碱基序列的非核素标记的核酸探针,依据碱基配对原理,通过免疫细胞化学检测体系,在组织切片、细胞间期核或染色体等标本上,进行DNA定性、定位及定量分析。本法快速、安全、灵敏度高,特异性强。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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