FRAGILE X (FMR1) MUTATION SCREEN

  • Test Usage:
    Mutations in the FMR1 gene cause fragile X syndrome. Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. This test is used to determine the number of time the CGG triplet is repeated to diagnose Fragile X syndrome.
  • Report Availability:
    Sample by Sat 11 am; Report 15 days
24 Diagnostic Centers found for FRAGILE X (FMR1) MUTATION SCREEN in Faridabad