Prenatal Carrier Screening Test | Inherited

This blood test panel screens for carrier status of three prenatal diseases: Spinal muscular atrophy (SMA), Fragile X Syndrome, and Cystic Fibrosis (CF).

About this test

The Prenatal Carrier Screening Test | Inherited is a laboratory test. Your health care provider can explain what it measures and whether it is appropriate for your situation.

· Turnaround: 1-3 business days · Preparation: Follow the lab's instructions.

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Order Prenatal Carrier Screening Test | Inherited

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