Wikipedia:WikiProject Council/Proposals/Neurofibromatosis
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- The following discussion is an archived proposal of the WikiProject below. Please do not modify it. Subsequent comments should be made on the appropriate discussion page (such as the project's talk page (if created) or the WikiProject Council). No further edits should be made to this page.
The resulting WikiProject was not created
Description[edit]
All related to description and treatment of NF-related conditions Erxnmedia (talk) 17:55, 27 May 2011 (UTC)[reply]
Support[edit]
Please specify whether or not you would join the project.
Discussion[edit]
- I would like to create a project focussing on Neurofibromatosis as it's own field. I have been updating NF-related pages and I find that my edits go unchallenged, which worries me. Here are NF-related pages that I have edited which I would tag with the NF project in the Discussion page if people like the idea:
- Café au lait spot
- Children's Tumor Foundation
- DNA sequencing
- GTPase
- Imatinib
- Lapatinib
- Legius syndrome
- List of cutaneous conditions
- Lovastatin
- Mutation
- Neurofibroma
- Neurofibromatosis
- Neurofibromatosis type I
- Neurofibromatosis type II
- Neurofibromin 1
- Peginterferon alfa-2a
- SPRED1 gene
- Schwannomatosis
- Solitary neurofibroma
- Sunitinib
- Tipifarnib
- Watson syndrome
Thanks, Erxnmedia (talk) 17:55, 27 May 2011 (UTC)[reply]
- The above discussion is preserved as an archive of the debate. Please do not modify it. Subsequent comments should be made on the appropriate discussion page (such as the project's talk page (if created) or at the WikiProject Council). No further edits should be made to this page.