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  1. Main Page ‎(208 revisions)
  2. Mutations: Changes in the Genome ‎(96 revisions)
  3. Curriculum Inversion for Better Classroom Genetics ‎(63 revisions)
  4. Chromosome Abnormality ‎(60 revisions)
  5. Mowat-Wilson Syndrome ‎(51 revisions)
  6. A-F ‎(50 revisions)
  7. How to Find Qualified Services ‎(48 revisions)
  8. Von Hippel-Lindau Syndrome ‎(47 revisions)
  9. Glossary of Genetic Terms and Concepts ‎(39 revisions)
  10. Genetics & Public Policy Center Reports Summaries ‎(36 revisions)
  11. Genetic Counseling ‎(35 revisions)
  12. Advocacy Organizations ‎(33 revisions)
  13. G-N ‎(32 revisions)
  14. O-U ‎(27 revisions)
  15. How to Get Started ‎(26 revisions)
  16. Newborn Screening ‎(25 revisions)
  17. Who's Who in Genetics - Professions & Credentials ‎(25 revisions)
  18. Newborn Screening Programs in New England ‎(24 revisions)
  19. Other ‎(24 revisions)
  20. Ethical, Legal, and Social Issues ‎(23 revisions)
  21. Start Using WikiGenetics ‎(23 revisions)
  22. Genetic Contributions to Health ‎(22 revisions)
  23. Cockayne Syndrome ‎(20 revisions)
  24. A Patient's Guide to Genetic Counseling ‎(19 revisions)
  25. Alpha Mannosidosis ‎(19 revisions)
  26. Chromosomes in Cells ‎(19 revisions)
  27. Isovaleric Acidemia ‎(19 revisions)
  28. Professional Societies ‎(19 revisions)
  29. Alagille Syndrome ‎(18 revisions)
  30. American Society of Human Genetics ‎(18 revisions)
  31. Barth Syndrome ‎(18 revisions)
  32. Lou Gehrig Disease ‎(18 revisions)
  33. Xanthogranuloma, Juvenile ‎(18 revisions)
  34. 46,XY,del(9)(q31.2q33.1) ‎(17 revisions)
  35. Family History ‎(17 revisions)
  36. Genetic Alliance ‎(17 revisions)
  37. Vision for the Future: Public and Professional Education and Community Engagement in Genomics ‎(17 revisions)
  38. Vitiligo ‎(17 revisions)
  39. Basic Formatting ‎(16 revisions)
  40. Genes and Their Properties ‎(16 revisions)
  41. Huntington's Disease ‎(16 revisions)
  42. Marinesco-Sjogren Syndrome ‎(16 revisions)
  43. Organization of the Human Genome ‎(16 revisions)
  44. VLCAD Deficiency ‎(16 revisions)
  45. Patient Stories and Consumer Profiles ‎(15 revisions)
  46. Spinal Muscular Atrophy (SMA) ‎(15 revisions)
  47. Holoprosencephaly ‎(14 revisions)
  48. Velocardiofacial Syndrome (VCFS) ‎(14 revisions)
  49. Wolff-Parkinson-White Syndrome ‎(14 revisions)
  50. Zellweger Syndrome ‎(14 revisions)

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