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  • Home
  • About Us
    • Mission
    • Staff
    • Advisory Committee
    • Current Activities
    • Partners
      • NERGG and NERGN - What's the Difference?
      • Other Regional Genetics Networks
    • Evaluation
    • Contact Us
  • News
    • Newsletters
  • Events
    • ECHO Series
    • Genetic Webinars
    • Annual Meeting
  • Resources
    • Genetic Education Support System (GESS)
    • Resource Library
      • Navigating Insurance & Appeals
      • Letters of Medical Necessity
      • Newborn Screening
    • Find Services
    • COVID-19 Resources
  • Contact Us
    • Staff
    • Directions
    • Join our Mailing List

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News

Tuesday, August 6, 2019
Point of View: An evolution from genetic counselling to genomic counselling
Tuesday, July 16, 2019
Following up on Positive Newborn Screening Results
Tuesday, June 18, 2019
NIH director will no longer speak on all-male science panels
Monday, June 17, 2019
The Unfulfilled Promise of DNA Testing
Tuesday, May 28, 2019
The choice not to undergo genetic testing for Huntington disease: Results from the PHAROS study.
Thursday, May 2, 2019
Vermont Adds Four New Conditions to Newborn Screening Panel
Thursday, May 2, 2019
Take Action to Support Newborn Screening - Message from NORD
Monday, April 15, 2019
ACP Survey Shows Physician Interest in Implementing Telehealth
Thursday, April 11, 2019
Does Genetic Testing Affect Your Life Insurance?
Tuesday, April 9, 2019
Defining the Responsibility to Recontact Research Participants with New Genetic Findings

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The New England Regional Genetics Network is supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) as part of an award totaling $600,000 with 0% financed with non-governmental sources. The contents are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by HRSA, HHS, or the U.S. Government. For more information, please visit HRSA.gov.