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Showing below up to 50 results in range #1 to #50.

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1. Registry Questionnaires‏‎ (1 revision)
2. Speaker selection and management‏‎ (1 revision)
3. Available Resources‏‎ (1 revision)
4. Consumers and Researchers: Making It Work‏‎ (1 revision)
5. Editing Practice‏‎ (1 revision)
6. Getting a Biobank or Registry Started‏‎ (1 revision)
7. Meet Your Neighbors & Organizations‏‎ (1 revision)
8. Phone Services: Going Beyond the Phone Tree‏‎ (1 revision)
9. Registry and Biobank Ethics and Governance‏‎ (1 revision)
10. Characterize Condition‏‎ (1 revision)
11. Cool Tips‏‎ (1 revision)
12. Funding‏‎ (1 revision)
13. Getting an ICD-9 code added for your condition‏‎ (1 revision)
14. Internet Services‏‎ (1 revision)
15. Member Dues‏‎ (1 revision)
16. Planning a Research Conference‏‎ (1 revision)
17. Accepting Donations‏‎ (1 revision)
18. Basic Formatting‏‎ (1 revision)
19. Characterize Resources‏‎ (1 revision)
20. Councils and Other Advisory Bodies‏‎ (1 revision)
21. Educating Your Membership about Research‏‎ (1 revision)
22. Funding Research by Others‏‎ (1 revision)
23. Harnessing the Resources That Are Hard to Measure‏‎ (1 revision)
24. Mentors‏‎ (1 revision)
25. Policy Tools & Resources‏‎ (1 revision)
26. Research Model 1: Recessive Disorder‏‎ (1 revision)
27. Starting Points for Planning Materials‏‎ (1 revision)
28. Working Full-Time on Nonprofit‏‎ (1 revision)
29. Accessibility of Tools‏‎ (1 revision)
30. Becoming the Organization You Imagine‏‎ (1 revision)
31. Creating New Pages‏‎ (1 revision)
32. Education of Members, Providers, and the Public‏‎ (1 revision)
33. Health care Providers and Specialists‏‎ (1 revision)
34. NAC Best Practices‏‎ (1 revision)
35. Preparing for and Handling Publicity‏‎ (1 revision)
36. Research Model 2: Chromosomal Disorder‏‎ (1 revision)
37. State-Specific Issues‏‎ (1 revision)
38. Creating a Natural History Survey‏‎ (1 revision)
39. Emergency Preparedness‏‎ (1 revision)
40. Internet Services: Websites, Chat Rooms, and Newsgroups‏‎ (1 revision)
41. National Awareness Day‏‎ (1 revision)
42. Press Kits‏‎ (1 revision)
43. Research Model 3: Dominant Disorder‏‎ (1 revision)
44. Additional/Supplemental Resources‏‎ (1 revision)
45. History of Advocacy Organizations and Genetic Alliance‏‎ (1 revision)
46. National Institutes of Health (NIH)‏‎ (1 revision)
47. Promoting Research‏‎ (1 revision)
48. Research Models‏‎ (1 revision)
49. Choosing Internet Service Provider‏‎ (1 revision)
50. Events‏‎ (1 revision)

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