Leadership Workshop
Organizational Development Workshop
Research Symposium
Policy Symposium
Community Screening and Counseling for Sickle Cell Disease
The Challenges and Rewards of Developing, Maintaining, and Translating Disease-Specific Facts Sheets for Parents
Collaborating for Genetics Education: Roadblocks and Rewards
Bringing Social Justice to Genetic Technologies
Using Family History to Improve Your Health: A School-Based Approach for Reaching Students and Families
Newborn Screening: Joint Responsibilities
Making the Most of Your Educational Materials
The Power of Youth: Nurturing Next Generation Leaders
Crossing All the T's: Translating Human Genomics Discoveries into Population Health Benefits
Family History for Communities: Creating a Unique Tool
Assuring Quality in Parent to Parent Support Services
Patient Empowerment: Research and Experience
Coverage and Reimbursement: The Ultimate Hurdles
After the Screening: Assuring Long-Term Follow-Up After Diagnosis Through Newborn Screening
Nutrition and Genetics: Translating Science to Practice
Electronic Health Records: What's happening and why you should be involved
Family Networking and Leadership
De-identified Samples: The Humanity of it All
Education and Resources for the Public about Rare and Common Genetic Disorders: A Trans-NIH Approach