New England Regional Genetics Network

News

Monday, January 14, 2019

Early Identification of Fragile X Syndrome through Expanded Newborn Screening

Monday, January 7, 2019

Should pretest genetic counselling be required for patients pursuing genomic sequencing?

Monday, January 7, 2019

Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families.

Tuesday, December 18, 2018

Developing a Process for Returning Medically Actionable Genomic Variants to Latino Patients in a Federally Qualified Health Center

Monday, December 10, 2018

The Ethics of Heritable Genome Editing New Considerations in a Controversial Area

Tuesday, December 4, 2018

Thought leader perspectives on benefits and harms in precision medicine research

Tuesday, December 4, 2018

Newborn Screening for Severe Combined Immunodeficiency in the United States: Lessons Learned

Monday, November 26, 2018

NCI-MATCH Update: More Labs, New Arms, and Initial Findings

Tuesday, November 13, 2018

Foundation of the Newborn Screening Translational Research Network and its tools for research

Tuesday, November 13, 2018

Striving for Precision: Enhancing Genetic Competency in Primary Care Nurse Practitioner Students.

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