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