About this test
Rapid detection of common aneuploidies (chromosomes 13, 18, 21, X, Y).
Parameters
A parameter breakdown is not available for this entry. Contact the centre for the exact investigation details.
Sample & preparation
- Sample
- Specimen-specific: POC / amniotic fluid / blood as advised
- Preparation
- Written consent and pre-test counselling; bring family history and prior reports. Prenatal procedures: Form F (PC&PNDT).
Confirm preparation and reporting time with OnePLUS when booking. Your referring clinician can advise which investigation is appropriate.
