FRAGILE X (FMR1) MUTATION SCREEN
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.
Parameter(s) covered : 2
Report Frequency: Sample Mon by 9 am; Report Fri
Special Instruction: Physician prescription is mandatory.
Price : ₹ 8100.00
Parameters
- Fragile X
- KINDLY NOTE