Public health, health services and implementation

985 - Determining the Prevalence and Family History of Noncommunicable Diseases at Korle Bu Teaching Hospital using the MiGene Family History App

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984 - A Genomic Future for Newborn Screening: Sequencing a Baby for an Optimal Outcome

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988 - Increasing Diversity Among Genetic Professionals to Improve Access to Genetic Services for Underserved Minority Communities
994 - The Clinical Utility of Genomic Sequencing Across Clinical Indications: A Systematic Review
995 - Training and Tools to Empower Non-Genetics Providers to Return Genome Sequencing Results in the NICU Setting
997 - Cancer Patients’ Preferences on Being Re-contacted with Updated Genomic Results
999 - Inclusion of employer-based and geographic attributes in value assessment methods of next-generation sequencing tests
1000 - One Year Later: Experiences Adding Three New Disorders to Newborn Screen in the District of Columbia
1002 - Biorepository Development within an Integrated Health Care System: Barriers and Facilitators
1003 - Prevalence of muscular dystrophy in Korea: a population-based study using the national health insurance claims database
1005 - DNA Based Newborn Screening: Establishing a Program for Targeted Mutations in the Amish Population
1006 - Early Recruitment and Enrollment in a Genomic Medicine Clinical Trial Focused on Underserved and Under-represented Populations: NCGENES 2