GTLDNA offers a range of cutting-edge and highly scientific genetic tests which fall under our clinical and molecular testing portfolio.
We are pleased to announce a very Special Prenatal Package which includes our Non Invasive Prenatal Paternity Test, Non Invasive Prenatal Screening Test for Down’s Syndrome and many other Chromosomal Disorders and also our baby gender test. Below, find a short description to each test. Contact us for more information.Order Now More Info
‘Prenatal Peace’ – Non-Invasive Prenatal Genetic Screening Test
GTLDNA can now offer the most comprehensive non-invasive prenatal genetic screening test available – Our ‘Prenatal Peace’ (also called NIFTY™) test is a 100% safe test that screens for Down’s syndrome and 17 other genetic conditions. Starting at just 10 weeks of pregnancy and using only a maternal blood sample, this test can provide more accurate results compared to traditional screening methods. This test also includes Gender Determination upon request for no extra charge.Order Now More Info
Newborn Genetic Test with NOVA™
Postnatal Peace is proud to be able to offer Nova™.
Nova™ is a newborn screening test that determines a baby’s risk for 50 inherited disorders, as well as providing personalised genetic information on the metabolism of 20 drugs. Nova™ utilises Next Generation sequencing technology, coupled with the leading genetics bioinformatics software. Postnatal peace is able to offer the most comprehensive and accurate newborn screening test that is over 99.99% accurate.Order Now More Info
Inherited Diseases Panel
Cancer Panel Genetic Predisposition Test
Establish your genetic risk of hereditary cancers. We offer a cancer panel test which will look for a total of 92 mutations associated with hereditary cancers.More Info
Inherited Cancer Panel
Our Inherited Cancer Panel specifically looks for inherited gene mutations in over 130 different genes associated with a wide range of hereditary cancers (including BRCA1, BRCA2 & PALB2). This screening test can be used to identify gene mutations responsible for hereditary cancers and to clarify the genetic risk for individuals with a family history of these hereditary cancers. It is a powerful tool that can help you reduce your risks or undertake measures that will help you detect hereditary cancers as early as possible.Order Now More Info