Detects genetic mutations associated with hereditary persistence of fetal hemoglobin…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
HPFH
9,713 THB
SKU :
MD-NLA216
Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.
Lab Categories : All Ages, Amniotic Fluid, Anemia, Blood, Family History, Fatigue, Gap PCR, Genetic Disorders, Lab Test
Diseases : Genetic Disorders
Habits : Family History
Age Groups : All Ages
Specimens : Amniotic Fluid, Blood
Diagnostic Methods : Gap PCR
| Also Known As | HPFH Gene Mutation Test |
|---|---|
| Specimen | EDTA whole blood 6 ml. or Amniotic fluid 10 ml. |
| Turnaround Time | 23 days |
| Test Code | MD-NLA216 |
| Test Type | Special |
| Related Tests | Genetic Disorder Panel |
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