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Maggie's Family Website
Beskrivning: 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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språk: English
Site ämnen: conditions
Angelman Syndrome Foundation, Inc: The Angelman Syndrome Foundation’s mission is to advance the awareness and treatment of Angelman Syndrome through education and ...
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3.0 / 5.0, språk: English
Information and links concerning Dopa-Responsive Dystonia (aka Segawa's Disease)
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3.0 / 5.0, språk: English
Angelman Syndrome (AS) is a rare neuro-genetic disorder named after an English paediatrician, Dr. Harry Angelman, who first described the syndrome in 1965. A ...
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Describes the Southern blot test used in diagnosis.
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Learn about careers
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Informational resources on specific diagnoses, communication connections, adaptive products and technology, adaptive recreational activities, education, worship ...
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Foundation that raises money and awareness about the debilitating movement disorder, dystonia. Chronicles the journey of a brave young boy as he battles this ...
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ASSERT is a United Kingdom based support group. We are all volunteers who have direct contact with people with Angelman Syndrome. The majority of the trustee's are ...
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3.0 / 5.0, språk: English
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liknande webbplatser till Tremoraction.Org
liknande webbplatser till Pmdi.Org
liknande webbplatser till En.Wikipedia.Org
liknande webbplatser till Movementdisorders.Org
Wemove.Org alternativ
Cmdg.Org alternativ
Donnawilliams.Net alternativ
Aboutbfs alternativ
Pspinformation alternativ