FISH (Fluorescence in situ hybridization) is a genetic test used to detect deletions and duplications, numerical and structural chromosomal anomalies.

Why FISH?

FISH has increased resolution as compared to a Karyotype test for targeted chromosomal abnormalities .

  •         A child with developmental disability
  •         Diagnosis of genetic disorders such as Prader Willi, Angelman syndrome and Down syndrome and other targeted chromosomal  abnormalities
  •         To diagnose, evaluate prognosis and remission of disease in certain cancers like breast cancers
  •     Sex Chromosomal Abnormalities

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