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Fibroblast Growth Factor receptor 2 gene
SKU: MD-NLB045 Categories: , , , , , , Tags: , , ,

In Stock

Fibroblast Growth Factor receptor 2 gene

฿7,245.00

Additional information

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

Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.

Product tags: Bone Deformities, Family History, FGFR2 Gene Sequencing, Genetic Disorders
Diseases: Genetic Disorders
Symptoms: Bone Deformities
Habits: Family History
Age Groups: Pediatric
Specimens: Blood
Diagnostic Methods: DNA Sequencing, PCR
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Description

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.

Additional information

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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