Carrier screening to help detect the risk of having a baby with a specific inherited disorder, such as cystic fibrosis.
Analyzes chromosomes in newborns and infants for changes that can explain certain birth defects or developmental delays.
Multiple testing options providing information on the genetic health of your baby during the first and second trimesters.
Genetic testing to help determine whether you have a mutation that increases your risk to develop certain cancers.
Diagnostic testing to help understand why a miscarriage occurred and the potential risk with future pregnancies.
If you’re a healthcare provider, you’re in the right place. If you’re a current or future patient, click the link below.