If you are already pregnant and you suspect your baby could have a genetic disease, we can help you rule it out with Clarix. It can help us detect genetic disorders associated with an imbalance in the number of chromosomes in your baby, we can perform it from week 10 and all we need is a blood sample from you. It is a Non-Invasive Prenatal Genetic Test since it reduces the need to extract amniotic fluid for analysis. With Clarix we analyze 5 chromosomes associated with the most common numerical genetic diseases compatible with life, such as: Down syndrome, Patau, Edwards, Turner, Klinefelter, Jacobs, and Triple X.
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