New England Regional Genetics Network

News

Monday, January 28, 2019

Racial and ethnic differences in knowledge and attitudes about genetic testing in the US: Systematic review.

Tuesday, January 22, 2019

Genetic testing is the future of healthcare, but many experts say companies like 23andMe are doing more harm than good

Monday, January 14, 2019

Integrating Genomics into Healthcare: A Global Responsibility

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

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