Health Testing by Integrated Genetics

Analyses every one of your baby’s chromosomes to identify any abnormalities.

• Noninvasive, prenatal, genome-wide testing
• Can be taken 10 weeks into pregnancy
• Must be approved and supervised by a doctor

Analyses your baby’s DNA to determine the risk of Rh blood type incompatibility between you and your baby.

• Noninvasive genotyping, laboratory-developed test
• Determines the RHD status of your baby through a blood sample
• Must be approved and supervised by a doctor

Analyses your baby’s chromosomes to screen for Down syndrome, Edwards’ syndrome, Patau syndrome, and many other conditions

• Can be taken as early as 10 weeks into pregnancy
• Can help ensure that your baby receives the proper care immediately
• Must be approved and supervised by a doctor

Analyses your DNA, providing information to identify if you are carriers of genetic disorders.

• Provides information regarding risks of having a pregnancy affected with certain inherited disorders
• Identifies carrier status for more than 110 genetic disorders
• Must be approved and supervised by a doctor