Skip Ribbon Commands
Skip to main content
  Print Page

Down Syndrome: National Conference on Patient Registries, Research Databases, & Biobanks

Skip sharing on social media links
Share this:

December 2-3, 2010


Intellectual and Developmental Disabilities (IDD) Branch, NICHD; Global Down Syndrome Foundation


Neurosciences Building, 6001 Executive Boulevard, Rockville, Maryland


This conference brought together leaders in the fields of Down syndrome clinical care, advocacy, and research, along with federal partners, including the NICHD. The goal of the meeting was to formulate a strategy for establishing and/or integrating patient registries, research databases, and biobanks into Down syndrome research to further advance the science and clinical trials that will benefit individuals with Down syndrome and their families.

For More Information


Dr. Melissa Parisi, IDD Branch, NICHD
Tel: (301) 496-1383

Last Updated Date: 11/30/2012
Last Reviewed Date: 11/30/2012