Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome…. 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 2 gene
Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
7,245 THB
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Lab Categories : Blood, Bone Deformities, Family History, Genetic Disorders, Lab Test, PCR + DNA Sequencing, Pediatric
Diseases : Genetic Disorders
Symptoms : Bone Deformities
Habits : Family History
Age Groups : Pediatric
Specimens : Blood
Diagnostic Methods : DNA Sequencing, PCR
| Also Known As | FGFR2 Gene Sequencing |
|---|---|
| Specimen | EDTA whole blood 10 ml (minimum 6 ml) |
| Turnaround Time | 30 Days |
| Test Code | MD-NLB045 |
| Test Type | Special |
| Related Tests | Genetic Panel |
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