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Chromosome study (blood)(MGC)
SKU: MD-NLB511 Categories: , , , , , , , , , Tags: , , , , ,

In Stock

Chromosome study (blood)(MGC)

฿3,640.00

Additional information

Also Known As

Karyotyping
Specimen

Heparinized blood 3 ml or cord blood 3-5 ml
Turnaround Time

16 days
Test Code

MD-NLB511
Test Type

Special
Related Tests

Genetic Testing, Prenatal Screening

Analyzes chromosomes for structural abnormalities, such as translocations, deletions, or duplications, which can lead to genetic conditions like Down syndrome or Turner syndrome.

Product tags: Chromosomal Abnormalities, Congenital Abnormalities, Developmental Delays, Genetic Disorders, Karyotyping, None
Diseases: Chromosomal Abnormalities, Genetic Disorders
Symptoms: Congenital Abnormalities, Developmental Delays
Habits: None
Age Groups: All Ages
Specimens: Cord Blood, Heparinized Blood
Diagnostic Methods: Cell Culture and G-Banding
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Description

Analyzes chromosomes for structural abnormalities, such as translocations, deletions, or duplications, which can lead to genetic conditions like Down syndrome or Turner 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

Karyotyping
Specimen

Heparinized blood 3 ml or cord blood 3-5 ml
Turnaround Time

16 days
Test Code

MD-NLB511
Test Type

Special
Related Tests

Genetic Testing, Prenatal Screening

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