FISH FOR ANGELMAN SYNDROME - (Outlab)
What does FISH FOR ANGELMAN SYNDROME - (Outlab) measure?
This genetic test uses fluorescence in situ hybridization (FISH) to examine the chromosome 15 region associated with Angelman syndrome for specific deletions or rearrangements. It may be used when a healthcare professional is evaluating developmental concerns or other clinical features that could be associated with this condition. Results are interpreted together with medical history, examination findings, and, when needed, other genetic tests.
This overview is educational. Use the recorded preparation, sample and lab-partner details below for collection guidance, and confirm any missing information before collection.
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Prices, report times and availability are shown from the catalog records for each eligible partner.
- Sample for analysis
- Confirm with the collection team
- Report time
- To be confirmed
Preparation and specimen requirements can vary by test and laboratory. Follow the instructions shown for your selected partner and any advice from your healthcare professional.