A comprehensive cardio-specific genetic test that determines your compatibility with drugs used in the treatment of cardiovascular disease.
Tests for abnormalities in the number or size of all the 23 chromosomes present in the cell. It is also able to determine the sex of the baby.
NeoBona GenomeWide provides a complete view of the fetal genome by analysing all 23 pairs of chromosomes to expand screening to other rare chromosomal abnormalities.
Analysis of 90 genetic variants present in 65 genes and 17 biochemical parameters
This test uses your genetic and biochemical profile to help to identify your unique nutritional needs for optimal health and disease prevention.
