Our Mission
The Disorders of Chromosome 16 Foundation (DOC16) is dedicated both to promoting research and providing information on chromosome 16 abnormalities.
The Foundation provides information, education, and support to families of children
living with a chromosome 16 disorder and to expectant parents confronting
a similar diagnosis. The Foundation also serves as a resource aiding
family, friends, caregivers, and medical professionals in their supportive roles.
Reaching Out
DOC16 is the only organization specifically for Chromosome 16 related disorders. We provide a wide range of educational and support services including:
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Web site
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Support via telephone and email
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Information on current research
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Referrals to other affected families
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Information for medical professionals
Board of Directors
President
Samantha Hubbell
Treasurer and Secretary
Marc Rosenstock
Members
Gina Haney
Wayne Lange
Gayle Timlin, M.S.W.
Medical Advisors
Peter A. Benn, Ph.D.
Director, Human Genetics Laboratories
Professor, Department of Pediatrics
University of Connecticut Health Center
Connecticut
Beth A. Pletcher, M.D., FAAP, FACMG
Associate Professor of Pediatrics
UMDNJ - New Jersey Medical School
New Jersey
Wendy P. Robinson,Ph.D.
Professor of Medical Genetics
B.C. Research Institute for Children's and Women's Health
Vancouver, B.C.
See Also: Frequently Asked Questions About the DOC16 Foundation
Disclaimer:
The Foundation respects each family's personal decisions. Information provided is for educational purposes only and should not be used for diagnosis, treatment or as a substitute for informed medical care.