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Fanconi (13)

See Also:
This category in other languages:

French

Sites:

http://www.alexandmatt.com
» Alex and Matt Pearl Open in a new browser window
   Personal stories of two children fighting Fanconi Anemia.
   http://www.alexandmatt.com
http://health.groups.yahoo.com/group/blackfan/
» Blackfan Open in a new browser window
   Yahoo list group for Diamond Black Fan Anemia sufferers.
   http://health.groups.yahoo.com/group/blackfan/
http://www.familyvillage.wisc.edu/lib_fanc.htm
» Family Village: Fanconi Anemia Open in a new browser window
   Features contact information for the Fanconi Anemia Research Fund. Links to personal accounts and areas where one can learn about the disease.
   http://www.familyvillage.wisc.edu/lib_fanc.htm
http://health.groups.yahoo.com/group/fanconi/
» Fanconi Open in a new browser window
   Yahoo list group for sufferers of this condition.
   http://health.groups.yahoo.com/group/fanconi/
http://www.members.cox.net/amgough/Fanconi.shtml
» Fanconi Anemia Open in a new browser window
   Discusses the genetics of this condition and treatment options.
   http://www.members.cox.net/amgough/Fanconi.shtml
http://www.mazornet.com/genetics/fanconi_anemia.htm
» Fanconi Anemia Fact Sheet - Jewish Genetic Diseases Open in a new browser window
   Fact Sheet on this anemia with emphasis on FANC-C variant of disease being a Jewish Genetic Diseases, including support resources.
   http://www.mazornet.com/genetics/fanconi_anemia.htm
http://www.fanconi.org/
» Fanconi Anemia Research Fund Open in a new browser window
   To find effective treatments and a cure for this disease, and to provide education and support services to affected families worldwide.
   http://www.fanconi.org/
http://members.tripod.com/fanconianemiaweb/
» Fanconi Anemia Web Open in a new browser window
   An informational site for this disorder.
   http://members.tripod.com/fanconianemiaweb/
http://www.fanconicanada.org/
» Fanconi Canada Open in a new browser window
   Canadian charity whose mission is to fund medical research into finding a cure for Fanconi Anemia and to serve as a support network for affected Canadian families.
   http://www.fanconicanada.org/
http://www.worthyfs.com
» Fanconi Syndrome Open in a new browser window
   Read how Markita Worthy celebrated her 31st birthday, having Fanconi's syndrome for 29 of those years. Also offers information about this rare disorder and links to further resources.
   http://www.worthyfs.com
http://www.socialstyrelsen.se/en/rarediseases/Fanconi%2banaemia.htm
» Fanconi anaemia in the Swedish Rare Disease Database Open in a new browser window
   Information text in English about Fanconi anaemia from the Rare Disease Database of the Swedish National Board of Health and Welfare
   http://www.socialstyrelsen.se/en/rarediseases/Fanconi%2banaemia.htm
http://www.katafoundation.org
» KATA Foundation Open in a new browser window
   The Kendall and Taylor Atkinson Foundation (KATA) raises funds to support scientific and medical research of effective treatments and a cure for Fanconi anemia
   http://www.katafoundation.org
http://www.kapsforkendall.com
» Kaps for Kendall Open in a new browser window
   In memory of Kendall Atkinson who died of Fanconi Anemia. Make or sponsor a hat that will be donated to children and adults in cancer and hematology treatment centers.
   http://www.kapsforkendall.com

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Last Updated: 2010-07-15 18:29:15





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