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.
FISH for DiGeorge/VCFS TUPLE1 syn- drome(22q11)
Detects 22q11 deletion associated with DiGeorge syndrome using FISH.
8,463 THB
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Lab Categories : Children, DiGeorge Syndrome, FISH, Heart Defects, Heparinized Whole Blood, Immune Deficiency, Infants, Lab Test, None, Velocardiofacial Syndrome
Diseases : DiGeorge Syndrome, Velocardiofacial Syndrome
Symptoms : Heart Defects, Immune Deficiency
Habits : None
Specimens : Heparinized Whole Blood
Diagnostic Methods : FISH
| 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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