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CDO is a registered 501C3 non-profit organization. For over 31 years we have been providing support and information to all those affected by the rarest chromosome and gene disorders. We offer personalized matching and research programs, parent to parent networking support and maintain a highly detailed database registry. Please help us continue this vital work. Whether a diagnosis is received prenatally or when an adult, CDO always will be there to help individuals and their families. Alone we may go unnoticed, together our intensity cannot be missed. #youarenotalone
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