Feb. 13-14, 2006: National Coordinating Center for Genetics and Newborn Screening Regional Collaboratives
Agenda (PDF - 32KB)
Minutes (PDF - 346KB)
National Coordinating Center for Genetics and Newborn Screening Regional Collaboratives (PDF - 549KB)
Michael S. Watson, PhD, FACMG
Epidemiology: Mapping Genetic Needs Relative to Services for Cystic Fibrosis, Hemoglobinopathies and Metabolic Disorders (PDF - 265KB)
Anne Marie Comeau, PhD
Performance Metrics and Harmonization of Cutoff Values for Newborn Screening by Tandem Mass Spectrometry (MS/MS) (PDF - 1324KB)
Piero Rinaldo, M.D., Ph.D.
Genetic/Metabolic Health Care Delivery During and After Hurricanes Katrina and Rita (PDF - 15KB)
Jess Thoene, M.D.
Encouraging Research Into Rare Diseases – The Rare Diseases Clinical Research Network (PDF - 604KB)
Stephen C. Groft, Pharm.D.
Considering Disorders For NBS: Criteria Work Group Report of the Nominating and review process (PDF - 39KB)
Nancy Green, M.D.
A Trial Run of a Condition Using the Proposed Nomination Process (PDF - 576KB)
Piero Rinaldo, M.D., Ph.D.
Issues in Presymptomatic Diagnoses of Lysosomal Storage Diseases (PDF - 177KB)
Robert F. Vogt, Jr., Ph.D.
Newborn Screening: The Role of State Legislatures (PDF - 53KB)
Alissa Johnson, M.A.
Association of State and Territorial Health Officials (PDF - 16KB)
Christopher A. Kus, M.D., M.P.H.
Persons using assistive technology may not be able to fully access information in these files. For assistance, contact comments@hrsa.gov or 888-275-4772 (TTY: 877-489-4772).