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SMA carrier screening by real-time PCR and Fragile-X Syndrome and Cystic Fibrosis 139 (Genome star)
SKU: MD-NLMM078 Categories: , , , , , , , , , , , Tags: , , , , , , , , ,

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SMA carrier screening by real-time PCR and Fragile-X Syndrome and Cystic Fibrosis 139 (Genome star)

฿68,320.00

Additional information

Also Known As

SMA Carrier Test, Fragile X Test, Cystic Fibrosis Test
Specimen

EDTA whole blood 3 ml (3 tubes)
Turnaround Time

5 weeks
Test Code

MD-NLMM078
Test Type

Special
Related Tests

Genetic Carrier Screening, Whole Exome Sequencing

Comprehensive screening for genetic mutations associated with SMA, Fragile X syndrome, and cystic fibrosis.

Product tags: Cystic Fibrosis, Cystic Fibrosis Test, Developmental Delays, Fragile X Syndrome, Fragile X Test, Genetic Disorders, Muscle Weakness, None, SMA Carrier Test, Spinal Muscular Atrophy
Diseases: Cystic Fibrosis, Fragile X Syndrome, Genetic Disorders, Spinal Muscular Atrophy
Symptoms: Developmental Delays, Muscle Weakness
Habits: None
Age Groups: All Ages
Specimens: EDTA Whole Blood
Diagnostic Methods: NGS, Real-time PCR
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Description

Comprehensive screening for genetic mutations associated with SMA, Fragile X syndrome, and cystic fibrosis.

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

SMA Carrier Test, Fragile X Test, Cystic Fibrosis Test
Specimen

EDTA whole blood 3 ml (3 tubes)
Turnaround Time

5 weeks
Test Code

MD-NLMM078
Test Type

Special
Related Tests

Genetic Carrier Screening, Whole Exome Sequencing

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