Cytogenetic Analysis
Cytogenetics involves testing tissue, blood, or bone marrow samples in a laboratory to look for chromosome changes, including broken, missing, rearranged, or extra chromosomes. Changes in specific chromosomes may signify a genetic disease, condition or cancer. Cytogenetics may help diagnose a disease or condition, plan treatment, or find out how well the treatment works.
The Cytogenetics Laboratory performs chromosome analysis, fluorescence in situ hybridization (FISH), and single nucleotide polymorphism (SNP) microarray testing.
Molecular cytogenetics and genomic analysis are now integral diagnostic and prognostic tools in various branches of medicine (e.g., obstetrics/gynecology, pediatrics, cardiology, neurology, internal medicine, haematology, and oncology).
We provide state-of-the-art services with fast turnaround time and competitive prices.