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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

Monday, August 7, 2017
Genomic Justice and Imagined Communities
Monday, August 7, 2017
Will Healthcare Inequality Cause Genetic Diseases to Disproportionately Impact the Poor?
Monday, August 7, 2017
Building consensus on genomic data sharing
Tuesday, August 1, 2017
Discovery Documentary on the NIH Clinical Center
Monday, July 17, 2017
Tumor gene testing urged to tell if drug targets your cancer
Monday, July 17, 2017
Expanded Newborn Screening: Information and Resources for the Family Physician
Monday, July 17, 2017
Provision of Genetic Services for Autism and its Impact on Spanish Families
Friday, June 30, 2017
FDA unveils plan to eliminate orphan designation backlog
Friday, June 30, 2017
Mitochondrial disease has a disproportionate healthcare burden in US
Friday, June 30, 2017
What Mormon Family Trees Tell Us About Cancer

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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.