Newborn Screening

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New laboratory screening test for fragile X syndrome shortly after birth now ready for pivotal North Carolina Early Check clinical study

New NC-Based Study to Advance Research Through Free and Expanded Health Screening for Newborn Babies

Early Check genome sequencing study reaches milestone of over 1,000 newborns screened in North Carolina

RTI International and the North Carolina State Laboratory of Public Health edit a special issue of the North Carolina Medical Journal on newborn screening

Revvity to provide genome sequencing for North Carolina newborn screening study under deal with RTI

Triangle researchers announce ‘Early Check’ study that could improve health outcomes for NC newborns

Study: Children with Gene Mutation Associated with Fragile X Experience Developmental Delays in First Two Years of Life

North Carolina’s Early Check Program to Add New Muscular Dystrophy Test to Newborn Screening Panel

Pioneering studies show promise in sequencing a baby’s genome at birth

Holly Peay, PhD, on keeping patient preference in focus

Three Babies with Spinal Muscular Atrophy Have Bright Futures Thanks in Part to North Carolina’s Early Check Program

Commentary recommends improving process for adding conditions to newborn screening panels

Experts Call for Better Newborn Screening to Take Advantage of Novel Therapies

New Paper Describes Accurate, Scalable Method for Detecting Fragile X Syndrome in Newborns

SMA Added to North Carolina’s Newborn Screening Program

Publication Finds That Modernization of U.S. Newborn Screening System is Necessary, Identifies Strategies for Change

Reimagining the Newborn Screening System: Q&A with Don Bailey