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Fact Sheet
El consentimiento informado es más que un formulario; es un proceso. ¿Qué implica?
Recurso educativo
Instrucciones paso a paso y papel con pliegues para imprimir incluidos en el documento para descargar.
Fact Sheet
Genomic variation accounts for some of the differences among people, including important aspects of their health and susceptibility to diseases.
Policy Issues
The 9 steps a bill can go through before becoming a law, using the Genetic Information Non-Discrimination Act of 2003 as an example.
Outreach
The USA Science and Engineering Festival is an opportunity to take part in hands-on genetics and genomics activities.
Educational Resources
Step-by-step instructions and printable folding paper included in the downloadable document.
Event
On May 19-20, 2016, the National Human Genome Research Institute (NHGRI) hosted a two-day workshop where participants were asked to weigh the benefits and risks of sharing aggregate genomic data with secondary users.
Event
On April 16-17, 2018, the National Human Genome Research Institute (NHGRI) and the Eunice Kennedy Shriver National Institute of CHild Health and Human Development (NICHD) hosted a joint workshop - Genomic Medicine for Reproductive, Prenatal and Neonatal Health.
Event
As the National Institutes of Health’s Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT) program comes to a close, the NSIGHT program holds a public webinar on June 24, 2019, during its final steering committee meeting.
Event
On March 5-6, 2019, the Genomic Medicine Working Group hosted the Genomics in Health and Wellness Meeting in Bethesda, Maryland.