Newborn/Preconception Genetic Testing
Providing a healthy start for every new life
About newborn/preconception genetic testing
Our newborn/preconception genetic testing kits are advanced testing tools designed for testing laboratories and obstetrics and gynecology departments. The testing kits are to understand whether couples planning for pregnancy carry genetic disease gene mutations and to detect potential genetic disorders that may affect newborn health early on, providing valuable health information for families and physicians.
-
Wide coverage: The newborn/preconception genetic testing kits cover multiple common hereditary diseases, such as alpha/beta thalassemia, spinal muscular atrophy, fragile X syndrome, and hearing loss.
-
Rapid testing: Utilizing simple molecular biology techniques significantly reduces testing time.
-
Automated analysis: Paired with a one-stop data analysis solution, eliminating the need for manual interpretation.