Similar organisations to HUDSON-ALPHA INSTITUTE FOR
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Libraries, Library Science
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946.
New York Metropolitan Reference & Research Library Agency
METRO WORKS TO CREATE A SUSTAINABLE CULTURE OF CREATIVITY, COLLABORATION, AND OPEN EXCHANGE FOR LIBRARIES, ARCHIVES, MUSEUMS, AND CULTURAL INSTITUTIONS IN THE METROPOLITAN NEW YORK REGION AND AROUND THE WORLD.
New York City
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Cancer Research
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947.
John Happy Cll Research Foundation
Main page About Our Foundation About our Scientific Advisory Board Scientific Advisory Board Members Message from our President Useful Links About CLL Bulletin Board How You Can Help Contact us Chronic lymphocytic leukemia CLL is the most common form of leukemia in the Western Hemisphere and accounts for nearly 30 of all reported leukemias.
Denville
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Alliance/Advocacy Organizations
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948.
Team Telomere
An international community for telomere biology disorders.
4248
Coeur d'Alene
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Neurology, Neuroscience
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949.
Creutzfeldt-Jakob Disease Foundation Inc
Our mission is to support families and loved ones touched by CJD.
9873
Akron
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Diseases, Disorders, Medical Disciplines N.E.C.
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950.
North Carolina Medical Genetics Association
Meet the faces of genetic and genomic healthcare Its the people who make the North Carolina Medical Genetics Association great.
Greensboro
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Birth Defects, Genetic Diseases
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951.
Partners With Parc Inc
Our Mission: To empower people with intellectual and other developmental disabilities to achieve and experience the highest quality of life.
2983
Kingston
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International Migration, Refugee Issues
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952.
Hudson Valley Helps Refugees
Hudson Valley Helps Refugees Inc. SWEATS AND TSHIRTS ARE HERE.
Milton
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Fund Raising and/or Fund Distribution
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953.
The Telomere Project
The Telomere Project is dedicated to funding lifesaving efforts for those affected by telomere syndromes, in particular, idiopathic pulmonary fibrosis IPF The Telomere Project is dedicated to funding lifesaving efforts for those affected by telomere syndromes TS in particular those which result in shortened telomeres or low telomere promotion.
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Austin
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Brain Disorders
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954.
THE PIERCE FAMILY FRAGILE X FOUNDATION
The Pierce Family Fragile X Foundation is a non-profit created to fund research, development of treatments, and community awareness to find a cure for Fragile X Created to fund dedicated research, development of treatments, and community awareness for Fragile X The Pierce Family Fragile X Foundation is a nonprofit organization that has been created to fund dedicated research development of treatments and community awareness in support of finding a cure for Fragile X Syndrome affecting our beautiful boys Graham and Reid.
1717
WINCHESTER