The NNSGRC provides information and resources in the area of newborn screening and genetics to benefit health professionals, the public health community, consumers, and government officials.
The Center for Public Health and Community Genomics supports programs and activities related to genomics education in various settings from K-12 education through community education.
This agency serves as a focal point for all national program policies and operations related to Medicaid.
Michigan statistics developed from the collection of vital records ranging from events such as births, deaths, marriages, and divorces.
Reports and statistics from the MDCH Vital Statistics on infant mortality showing trends by county, city, and race.
This Strategic State Plan provides guidance to the Council regarding how it spends its resources and includes long-term goals to be accomplished within five years.
This notice describes how personal and medical information about you may be used and disclosed and how you can get access to this information.
A compilation of reports and fact sheets related to sudden cardiac death of the young, heart disease, and stroke in Michigan from the MDHHS Cardiovascular program.
The Michigan BioTrust for Health is an initiative to make leftover newborn screening samples more useful and available for medical or public health research. Explore the website for more information targeted towards new parents, health professionals, available consent options, and dried blood spot research.
