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Heritage Carrier Basic Thai Female panel (Thalassemia, SMA and Fragile X)
SKU: MD-NLMM235 Categories: , , , , , , , , , , Tags: , , , , , , ,

In Stock

Heritage Carrier Basic Thai Female panel (Thalassemia, SMA and Fragile X)

฿25,713.00

Additional information

Also Known As

Genetic Carrier Screening for Thalassemia, SMA, Fragile X
Specimen

EDTA whole blood 3 mL 2 tube
Turnaround Time

14 days
Test Code

MD-NLMM235
Test Type

Special
Related Tests

Genetic Carrier Testing, Thalassemia Panel

Screens for carrier status of common genetic conditions like Thalassemia, SMA (Spinal Muscular Atrophy), and Fragile X syndrome, which can be passed on to offspring.

Product tags: Carrier Screening, Family History of Genetic Diseases, Fragile X, Genetic Carrier Screening for Thalassemia, Genetic Disorders, Maternity, Preconception Planning, SMA
Diseases: Carrier Screening, Genetic Disorders
Symptoms: Family History of Genetic Diseases
Habits: Maternity, Preconception Planning
Age Groups: Adults, Women of Childbearing Age
Specimens: EDTA Whole Blood
Diagnostic Methods: Multiplex Gap-PCR, Sequencing
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Description

Screens for carrier status of common genetic conditions like Thalassemia, SMA (Spinal Muscular Atrophy), and Fragile X syndrome, which can be passed on to offspring.

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

Genetic Carrier Screening for Thalassemia, SMA, Fragile X
Specimen

EDTA whole blood 3 mL 2 tube
Turnaround Time

14 days
Test Code

MD-NLMM235
Test Type

Special
Related Tests

Genetic Carrier Testing, Thalassemia Panel

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