Resource Repository (ReRe)

NCC works with the seven Regional Genetics Networks (RGNs) and the National Genetics Education and Family Support Center (Family Center) towards our common mission of improving access to genetic services for underserved populations.  All nine organizations develop resources and tools to support this mission, which are compiled into the NCC Resource Repository (ReRe). ReRe contains resources from our system, as well as resources from partner organizations that can help us achieve our mission.

Find resources by topic area, resource type, language, and more by exploring ReRe below!

Resources

Would you like to see ReRe as a table? Please click here!

How To Use ReRe

Below is information on what type of information is in ReRe, as well as ways to contribute or be notified when a new resource is added to ReRe.

Resource Notification

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Submit A Resource

Is a resource missing? Submit your resource here.

Topics in ReRe

Awareness Campaign | Breastfeeding | Care Coordination | Careers | Condition Specific | Consumer Advocacy | COVID-19 | Education | Emergency Preparedness | Evaluation | Family Health History | Family Support | Genetic Service System | Genetic Test | Healthcare Access and Financing | Healthcare Interpreting | Long-Term Follow-Up | Medical Food | Medical Home | Newborn Hearing Screening | Newborn Screening | Pregnancy | Prenatal | State Specific | Tele-education | Telegenetics | Transition

Audience Resources Were Developed For

Administrators | Educators | Genetics Providers | Healthcare Interpreters | Insurers | Midwives | Non-Genetics Providers | Patients and/or Families | Policymakers | Public Health | Regional Genetics Networks | Researchers | Students | Title V Programs