Newborn Genetic Screening
Supporting Healthy Beginnings with Genetic Screening
NOVA™ Newborn Genetic Screening:
NOVA™ Newborn Genetic Screening Test determines a baby’s risk for 246 genes associated with 112 genetic diseases, including 254 disease subtypes including genetic metabolic diseases, deafness, immune deficiency diseases, Neuromuscular diseases (e.g. Duchenne Muscular Dystrophy, Spinal Muscular Atrophy etc.), and blood disorders such as thalassemia.
- NOVA™ Newborn Genetic Screening
- NOVA™ Metabolic Disease Screening.
- NOVA™ Newborn Hereditary Hearing Loss Screening
WHAT'S NEW
News & Updates
Discover recent achievements, healthcare updates, research highlights, and important announcements from ELC Biogen.
