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FISH for DiGeorge/VCFS TUPLE1 syn- drome(22q11)
SKU: MD-NLB135 Categories: , , , , , , , , , Tags: , , , , ,

In Stock

FISH for DiGeorge/VCFS TUPLE1 syn- drome(22q11)

฿8,463.00

Additional information

Also Known As

DiGeorge Syndrome FISH Test
Specimen

1. Hepariniz whole Blood 5 ml
Turnaround Time

16 days
Test Code

MD-NLB135
Test Type

Special
Related Tests

Genetic Disorder Panel

Detects 22q11 deletion associated with DiGeorge syndrome using FISH.

Product tags: DiGeorge Syndrome, DiGeorge Syndrome FISH Test, Heart Defects, Immune Deficiency, None, Velocardiofacial Syndrome
Diseases: DiGeorge Syndrome, Velocardiofacial Syndrome
Symptoms: Heart Defects, Immune Deficiency
Habits: None
Age Groups: Children, Infants
Specimens: Heparinized Whole Blood
Diagnostic Methods: FISH
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Description

Detects 22q11 deletion associated with DiGeorge syndrome using FISH.

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

DiGeorge Syndrome FISH Test
Specimen

1. Hepariniz whole Blood 5 ml
Turnaround Time

16 days
Test Code

MD-NLB135
Test Type

Special
Related Tests

Genetic Disorder Panel

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