The Resource Repository is a library of resources developed by the NCC, Regional Genetics Networks, and Family Center to increase access to quality genetic services for medically underserved populations.  There are also links to the ACT Sheets and Algorithms, as well as a nationwide directory of clinical genetics services.

Explore resources developed by the NCC, the seven regions, NGEFSC, and other national partners.  These resources can be sorted by topic, including: 

• • Care Coordination
  • Consumer Advocacy
  • Disease Specific
  • Education
  • Family Health History
  • Genetic Service System
  • Healthcare Access and Financing
  • Long-Term Follow-Up
  • Medical Food
  • Medical Home
  • Newborn Screening
  • Transition

Resources can also be sorted by target audience, such as Patients and/or Families, Genetics Providers, Non-Genetics Providers, Public Health, Educators, Policymakers, and Insurers.

https://nccrcg.org/resources/#Resource