For patients who are pregnant, the NIPT is a simple, safe and noninvasive way to screen for common chromosomal conditions.
Non invasive prenatal test brochure

While the NIPT is commonly known to screen for common chromosomal conditions such as Down syndrome, it is also used to detect microdeletions. Prenatal Screening: What are Microdeletions & Wh...

If your patients are ready to start a family, carrier screening can help determine the chances of passing a genetic disorder down to their children. Carrier Screening Test for couples planning a baby-0...

If your developing baby is born with a chromosomal mutation, that could result in he or she being diagnoses with a condition like DiGeorge Syndrome. medgenomeclariaindia

If you're expecting a baby, you may be wondering how the NIPT works. With just a simple blood test you can determine if Your baby will be born with a chromosomal condition. How Does NIPT Works.

If you’re pregnant, you want answers about your baby’s health as early as possible. NIPT gives you insights into your baby’s genetic health from as early as the 9th week of pregnancy. Prenatal Testing: Reassurance as Early as 9th Week o...

The NIPT, which can be taken as early as your 9th week of pregnancy, can help you determine the chances your baby will have a genetic condition. https://goo.gl/FPuaTR

Women who are expecting a baby should consider prenatal DNA testing to determine the chances of their babies being born with a common chromosomal condition. https://goo.gl/4GYgau

The NIPT process is actually quite simple! With just a blood test, you can determine the chances of your baby being born with a chromosomal condition. The NIPT Process: What You Need to Know

Accurately determine your risks of having a baby born with a chromosomal condition with just a simple blood test. The NIPT is safe, effective and poses no risks for you or your baby. Screen For Genetic Abnormalities During Pregnancy With The Nipt