Welcome healthcare providers! Because medical providers are the single most trusted source of health information for Michigan patients and families, this page was designed to help you find current resources on the topics of genetics and genomics that may be used to assist with family history collection, risk assessment and referral, or patient education. The resources listed in the highlighted box were specially selected for Michigan providers with additional resources listed below. For more information on a specific condition or topic of interest, use the site search.
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.
This Michigan act is to protect and promote public health and provide for the prevention and control of diseases and disabilities.
Guidelines provided by the National Heart, Lung, and Blood Institute (NHLBI) for managing sickle cell disease. This report is intended to assist healthcare professionals in their management of the disease among their infant, adolescent, and adult sickle disease patients.