pfond.cmmt.ubc.ca

PFOND | Home

Remember me on this computer. Developed by the Wasserman Laboratory. At UBC, PFOND is a web-based service to promote the sharing of information about research, treatment, and resources for rare genetic disorders. This is a list of our published sites. We have more sites in development! Visit sites under development. If you are impacted by a genetic disorder, you can look at the existing pages or let us know if your interests are not in PFOND yet. We’ll get on it as soon as we line up a volunteer.

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PFOND | Home | pfond.cmmt.ubc.ca Reviews

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Remember me on this computer. Developed by the Wasserman Laboratory. At UBC, PFOND is a web-based service to promote the sharing of information about research, treatment, and resources for rare genetic disorders. This is a list of our published sites. We have more sites in development! Visit sites under development. If you are impacted by a genetic disorder, you can look at the existing pages or let us know if your interests are not in PFOND yet. We’ll get on it as soon as we line up a volunteer.

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PFOND | Home | pfond.cmmt.ubc.ca Reviews

https://pfond.cmmt.ubc.ca

Remember me on this computer. Developed by the Wasserman Laboratory. At UBC, PFOND is a web-based service to promote the sharing of information about research, treatment, and resources for rare genetic disorders. This is a list of our published sites. We have more sites in development! Visit sites under development. If you are impacted by a genetic disorder, you can look at the existing pages or let us know if your interests are not in PFOND yet. We’ll get on it as soon as we line up a volunteer.

INTERNAL PAGES

pfond.cmmt.ubc.ca

1

Adams-Oliver Syndrome | Home

http://pfond.cmmt.ubc.ca/adamsoliversyndrome

Remember me on this computer. We're a fast growing community for individuals and families with rare genetic diseases. Come and be encouraged by others with stories like your own. If you would like to join us as a volunteer editor and help keep our pages up to date please navigate to our volunteer page. Case report of AOS management in a neonate. April 15, 2013. A new gene has been identified in individuals with Adams-Oliver Syndrome. April 15, 2013. April 25, 2012. May 2, 2011.

2

PFOND | Stub Sites

http://pfond.cmmt.ubc.ca/stub

Remember me on this computer. What are PFOND Stub Sites? Our Current List of Stub Sites. Infant Toxicity From Codeine. And Centre for Molecular Medicine and Therapeutics.

3

PFOND | Editor Package

http://pfond.cmmt.ubc.ca/editor-package

Remember me on this computer. Welcome to the PFOND Project! The following are two introductory videos. Here are some tasks that can help you become familiar with the system. Send a message to admin. With your registered username so your account can be granted editor access. Post comment to discussion boards. Add test links to the links section. Add test content to overview page. Setup RSS feed for PubMed. Setup RSS feed for Google News. Update the header image of your site. Questions, comments, concerns?

4

PFOND | PFOND Editor Manual

http://pfond.cmmt.ubc.ca/wiki/pfond-editor-manual

Remember me on this computer. First you need to create an account on PFOND by going to http:/ pfond.cmmt.ubc.ca/register. Send a message to admin ( http:/ pfond.cmmt.ubc.ca/members/admin/. With your registered username so your account can be granted editor access. We will try to keep this document as up to date as possible, but things may change as we are developing. Customizing your new site:. Change the front page image. Configure RSS feeds for your News Page. Configure your PubMed / Google RSS feeds.

5

Peter's Anomaly | Peters Anomaly | Home

http://pfond.cmmt.ubc.ca/peteranomaly

Remember me on this computer. We're a fast growing community for individuals and families with rare genetic diseases. Come and be encouraged by others with stories like your own. If you would like to join us as a volunteer editor and help keep our pages up to date please navigate to our volunteer page. Little ambassador – Avery. August 2, 2011. Briefly: Fundraiser set for firefighter’s newborn daughter. July 4, 2011. June 30, 2011. June 30, 2011. June 30, 2011. Most of our visitors.'.

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PFOND | Home

Remember me on this computer. Developed by the Wasserman Laboratory. At UBC, PFOND is a web-based service to promote the sharing of information about research, treatment, and resources for rare genetic disorders. This is a list of our published sites. We have more sites in development! Visit sites under development. If you are impacted by a genetic disorder, you can look at the existing pages or let us know if your interests are not in PFOND yet. We’ll get on it as soon as we line up a volunteer.

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