| EX0727 FRAGILE X (FMR1) MUTATION SCREEN |
| Specimen: |
4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. |
| Stability: |
| Room |
Refrigerated |
Frozen |
| 6 HRS |
1 WEEK |
NA |
|
| Method: |
TP-PCR, Fragment analysis |
| Comment: |
|
| Report: |
Contact us to know the TAT. |
| 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 times the CGG triplet is repeated to diagnose Fragile X syndrome. |
| Doctor Specialty: |
Neurologist |
| Disease: |
Genetic Disorders |
| Components: |
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| Courier Charges: |
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| Home Collection: |
Available (*T&C Apply) |
| Department: |
MOLECULAR DIAGNOSTICS |
| Pre Test Information: |
A duly filled Genomics Clinical Information Requisition Form is mandatory |
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