New Born Screening makes use of NGS technology, the All-in-one " multiplex PCR amplicon library preparation method. It performs complete exonic area sequencing for 130 genes linked to genetic and metabolic disorders. Children and babies should take the exam as the Panel that is capable of providing early genetic disease screening. This will provide essential knowledge for preventative management and early treatment diet recommendations. For the infant s general health and quality of life, early discovery, intervention, and care may be crucial. Call Now for Booking at 08800821778 | social@genes2me.com