December 13-14, 2010
Intellectual and Developmental Disabilities (IDD) Branch, Center for Developmental Biology and Perinatal Medicine (CDBPM), NICHD; National Human Genome Research Institute (NHGRI); Office of Rare Disease Research, NIH
5635 Fisher’s Lane, Rockville, Maryland
The purpose of the meeting was to identify elements of a trans-NIH research agenda that would lead to the application of new genomics concepts and technologies to newborn screening and child health. Attendees at the meeting included experts from academia, industry, and federal agencies in the fields of newborn screening and genomics.
Dr. Alan Decherney, PRAE, DIR, NICHDTel: (301) 496-5800E-mail: email@example.com
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