A blood test from 9 weeks of pregnancy to screen for Down Syndrome, Edward Syndrome and Patau Syndrome and many other genetic conditions. Detection rate for over 99%, false positive rate 1:1000. Fetal gender optional. Unlike other NIPT tests it screens all 46 fetal chromosomes and thus identifies an additional 30% of important genetic conditions which they would miss.
The MaterniT® GENOME laboratory-developed test is the only noninvasive prenatal test available to date that can analyze EVERY chromosome in your baby to identify extra or missing parts of chromosomes or whole chromosome changes—as early as 9+0 weeks into your pregnancy.
A complimentary early viability / growth scan is included.