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Fluorescence In Situ Hybridization and In Situ PCR

2011
The application of fluorescence in situ hybridization to chromosomes allows each member of the karyotype to be distinguished from all others. This technique can be used to detect changes in chromosomes. Individual genes and transgenes can be placed to chromosome as well.
James A. Birchler, Tatiana V. Danilova
openaire   +2 more sources

Fluorescence in situ hybridization in diagnostic cytology

Human Pathology, 2007
Fluorescence in situ hybridization (FISH) is a technique that uses fluorescently labeled DNA probes to detect chromosomal alterations in cells. FISH can detect various types of cytogenetic alterations including aneusomy (ie, abnormalities of chromosome copy number), duplication, amplification, deletion, and translocation.
Benjamin R. Kipp, Kevin C. Halling
openaire   +3 more sources

fluorescence in situ hybridization

2017
Fluorescence in situ hybridization (FISH) is a molecular cytogenetic technique used to physically map DNA sequences on chromosomes. In FISH, DNA probes are most often hybridized to target DNA in metaphase chromosomes spread on slides (in situ). FISH probes are variable in size.
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Clinical applications of fluorescence in situ hybridization

Genetic Analysis: Biomolecular Engineering, 1991
We review here the application of fluorescence in situ hybridization with chromosome-specific probes to chromosome classification and to detection of changes in chromosome number or structure associated with genetic disease. Information is presented on probe types that are available for disease detection.
Daniel Pinkel   +4 more
openaire   +3 more sources

Fluorescence In Situ Hybridization

Fluorescence in situ hybridization (FISH) is a macromolecule recognition technology based on the complementary properties of DNA or DNA/RNA double strands. Unlike most other techniques used to study chromosomes, FISH does not require actively dividing cells.
openaire   +1 more source

Fluorescence In Situ Hybridization in Oat

2017
This chapter describes methods to detect gene loci or gene transcripts by fluorescence labeling. Fluorescence in situ hybridization (FISH) can be used to identify the positions of genes or BACs or the distribution of repetitive sequences on metaphase chromosomes as well as the identification of alien chromosomes.
openaire   +3 more sources

Quantitative Fluorescence In Situ Hybridization (QFISH)

2016
Fluorescence in situ hybridization (FISH) has a wide spectrum of applications in current molecular cytogenetic and cancer research. This is a unique technique that can be used for chromosomal DNA analysis in all cell types, at all stages of the cell cycle, and at molecular resolution.
Ivan Y. Iourov, Ivan Y. Iourov
openaire   +2 more sources

Fluorescence in situ Hybridization (FISH)

2010
Fluorescence in situ hybridization (FISH) , Fluorescence in situ hybridization (FISH) , کتابخانه مرکزی دانشگاه علوم پزشکی ...
Emanuela V. Volpi, Joanna M. Bridger
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New Approaches to Fluorescence In Situ Hybridization

2006
Fluorescence in situ hybridization (FISH) is a nonisotopic labeling and detection method that provides a direct way to determine the relative location or copy number of specific DNA sequences in nuclei or chromosomes. With recent advancements, this technique has found increased application in a number of research areas, including cytogenetics, prenatal
Sabita K. Murthy, Douglas J. Demetrick
openaire   +3 more sources

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