Detects deletions or uniparental disomy associated with Prader-Willi 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.
Prader Willi Syndrome-FISH (DNA Center)
8,820 THB
SKU :
MD-NLB315
Detects deletions or uniparental disomy associated with Prader-Willi syndrome using FISH.
Lab Categories : Children, FISH, Genetic Disorder, Heparinized Whole Blood, Infants, Intellectual Disability, Lab Test, Obesity, Prader-Willi Syndrome
Diseases : Prader-Willi Syndrome
Symptoms : Intellectual Disability, Obesity
Habits : Genetic Disorder
Specimens : Heparinized Whole Blood
Diagnostic Methods : FISH
| Also Known As | Prader-Willi FISH Test |
|---|---|
| Specimen | Heparinized whole blood 3 ml |
| Turnaround Time | 16 days |
| Test Code | MD-NLB315 |
| Test Type | Special |
| Related Tests | Genetic Disorder Panel |
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