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This test was developed, and its performance characteristics determined, by Lab Corp.

It has not been cleared or approved by the US Food and Drug Administration (FDA). Sequenom collection kits are available, (People Soft #116373 379551G-CS-LCA. SEQUENOM-LCA ONLY KIT EA=1/KIT and People Soft #116374 549403G-CS-LCA.

cf DNA testing may not accurately identify fetal triploidy, balanced rearrangements, or the precise locations of subchromosomal duplications or deletions; these may be detected by prenatal diagnosis with CVS or amniocentesis.

The ability to report results may be impacted by maternal body mass index (BMI), maternal weight, and/or maternal systemic lupus erythematosus (SLE).

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