Programs
Advises the most appropriate application of universal screening tests, technologies, policies, guidelines and standards for effectively reducing morbidity and mortality in newborns and children having, or at risk for, heritable disorders.
CDC’s mission is collaborating to create the expertise, information, and tools that people and communities need to protect their health–through health promotion, prevention of disease, injury, and disability, and preparedness for new health threats.
A governmental program responsible for ensuring the health and well-being of the entire population of women, infants, and children.
A fundamental goal of the NCCRCG is to bring genetic services closer to local communities. The NCC provides infrastructure, coordination, technical assistance and resources necessary to address issues of universal importance, thereby avoiding duplication of efforts and allowing the regions to focus on their unique areas of need.
A database for pregnancy and other healthcare-related materials.
The medical research agency of the US Department of Health and Human Services.
The Newborn Screening Education Program provides healthcare professionals and institutions with certified learning opportunities to ensure that all well receive appropriate screening prior to discharge from the hospital.
