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Organizations Websites

- Category ID : 75937
1 -

Lysosomal Diseases New Zealand

Information, support and advocacy for families affected by Lysosomal Storage Diseases, a group of rare genetic diseases.
2 -

Hereditary Disease Foundation

Information about this non profit organization, news, newsletters, recommended reading and contact details.
3 -

Australian MPS & Related Diseases Society

Informs and support those affected, directly or indirectly by a mucopolysaccharide or related disease. Offers information regarding each disease, a discussion forum, a picture gallery and news of events.
4 -

Canadian Gene Cure Foundation

The CGCF supports excellence in core human genetics research and aims to raise funds to enable scientists to discover cures and treatments for genetic disorders. Find details about the programs and events, and contact information.
5 -

Telangiectasia Self Help Group

Provides several factsheets and a newsletter.
6 -

Genetic Alliance Group

Information about this UK umbrella group of organizations working together to improve services for people with genetic disorders. A notice board, education, services and links are provided.
7 -

Hereditary Hemorrhagic Telangiectasia Foundation International, Inc.

Provides patients, families, and doctors with educational information and fosters an exchange of information about the diagnosis and treatment of HHT between patients, physicians, researchers, genetic counselors, agencies, educators, and the general public.
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