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Support for families with a member with Angelman Syndrome in the UK. Newsletters and links to other AS sites.
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Information, links to other sites and personal accounts of living with Angelman syndrome. Includes a research paper on the subject written by the parent of an Angel.
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Australian couple chronicles their experience raising a child with Angelman Syndrome. Mailing list. General information.
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Explanation of the syndrome, information on homeschooling, and resources for families.
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Features a messageboard, photographs, and events calendar.
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Information from the Australian Angelman Syndrome Association.
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Information for doctors and families. Research, activities and groups.
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Offers information about the genetic disorder, AS. Also conference details, membership and contact.
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Providing support for families of children with angelman syndrome in Cantrebury, New Zealand. Includes events, international links and information about AS.
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Elijah has angelman syndrome and this is a weblog about him written by his Dad.
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Information about Angelman Syndrome from the University of Washington, Seattle.
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Follow the life of Maggie who was diagnosed in 2004 with angelman syndrome, a rare genetic disease. Includes details about AS, and a weblog.
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Describes the Southern blot test used in diagnosis.
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Definition, treatments, prognosis, and research information.
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Supports research on angelman syndrome. Find details about AS, projects, and scientific articles.
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A wry look on life with a newly diagnosed toddler with Angelmans Syndrome. UK site, but with some general links, both serious and humorous.
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Providing exchange of knowledge and experiences regarding the condition.
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An interactive database of videos, texts and photographs, with information for clinicians and families.
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Contacts, chat rooms, personal accounts and links.
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Collected information on Angelman Syndrome
