Patient's Bill of Rights

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< Patient's Bill of Rights

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The following pages link to Patient's Bill of Rights:

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• Main Page
• Part 2: Assessment and Development
• Functions of Advocacy Organization
• Education of Members, Providers, and the Public
• Getting Needs onto the Research Agenda
• Educating Membership about Research
• Genetic Privacy
• Promoting Research
• Funding Research by Others
• Barriers to Rare Disease Research
• Consumers and Researchers: Making It Work
• Benefits of Collaboration with Advocacy Organization Community
• Facilitating Quality Research
• Research Model 1: Recessive Disorder
• Research Model 2: Chromosomal Disorder
• Research Model 3: Dominant Disorder
• Blood and Tissue Banks
• Genetic Alliance BioBank
• Advocacy
• Research
• Education
• Support

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