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HPFH
SKU: MD-NLA216 Categories: , , , , , , , , Tags: , , , ,

In Stock

HPFH

฿9,713.00

Additional information

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

Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.

Product tags: Anemia, Family History, Fatigue, Genetic Disorders, HPFH Gene Mutation Test
Diseases: Genetic Disorders
Symptoms: Anemia, Fatigue
Habits: Family History
Age Groups: All Ages
Specimens: Amniotic Fluid, Blood
Diagnostic Methods: Gap PCR
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Description

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.

Additional information

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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