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chromosomal abnormalities
What Techniques are Used to Detect Chromosomal Abnormalities in Cancer?
Several advanced techniques are utilized to detect chromosomal abnormalities in cancer:
Karyotyping
: Visual examination of chromosomes under a microscope to identify large-scale changes.
Fluorescence In Situ Hybridization (FISH)
: Uses fluorescent probes to detect specific chromosome regions and identify abnormalities.
Comparative Genomic Hybridization (CGH)
: Assesses copy number variations across the genome.
Next-Generation Sequencing (NGS)
: Provides detailed insights into genetic mutations and rearrangements.
Frequently asked queries:
What are Chromosomal Abnormalities?
How Do Chromosomal Abnormalities Cause Cancer?
What Types of Chromosomal Abnormalities are Common in Cancer?
Which Cancers are Commonly Associated with Specific Chromosomal Abnormalities?
What Techniques are Used to Detect Chromosomal Abnormalities in Cancer?
How Do Chromosomal Abnormalities Influence Cancer Treatment?
What is the Prognosis for Patients with Chromosomal Abnormalities in Cancer?
Can Chromosomal Abnormalities be Prevented?
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