Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders…. 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.
Fibroblast Growth Factor receptor 3 gene
Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
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Lab Categories : All Ages, Amniotic Fluid, Blood, Family History, Genetic Disorders, Lab Test, PCR + Sequencing, Short Stature, Skeletal Abnormalities
Diseases : Genetic Disorders
Symptoms : Short Stature, Skeletal Abnormalities
Habits : Family History
Age Groups : All Ages
Specimens : EDTA whole blood or Amniotic fluid
Diagnostic Methods : PCR, Sequencing
| Also Known As | FGFR3 Mutation Test, Achondroplasia Test |
|---|---|
| Specimen | EDTA whole blood 10 ml or Amniotic fluid in sterile container |
| Turnaround Time | 2 months |
| Test Code | MD-NLB033 |
| Test Type | Special |
| Related Tests | Genetic Disorder Panel |
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