Developing standard names and codes for lysosomal storage disorders detectable by newborn screening
Rebecca M. Goodwin, JD1, Michael Watson, PhD, FACMG2, Dietrich Matern, MD, FACMG3, J. Gilbert Hill, MD, PHD4, Carla Cuthbert, PhD, FCCMG, FACMG5, Swapna Abhyankar, MD6, Sara Copeland, MD7, Tiina Urv, PhD8, Deboshree Sarkar, MPH9 and Clement McDonald, MD10
(1)Lister Hill National Center for Biomedical Communication, National Library of Medicine, National Institutes of Health, HHS, Bethesda, MD, (2)American College of Medical Genetics, Bethesda, MD, (3)Mayo Clinic College of Medicine, Rochester, MN, (4)electronic Child Health Network, Toronto, ON, Canada, (5)Centers for Disease Control and Prevention (CDC), Atlanta, GA, (6)National Library of Medicine, National Institutes of Health, Bethesda, MD, (7)Maternal and Child Health Bureau, Rockville, MD, (8)Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH, HHS, Rockville, MD, (9)Health Resources and Services Administration, HHS, Rockville, MD, (10)National Library of Medicine, National Institutes of Health, HHS, Bethesda, MD
(1)Lister Hill National Center for Biomedical Communication, National Library of Medicine, National Institutes of Health, HHS, Bethesda, MD, (2)American College of Medical Genetics, Bethesda, MD, (3)Mayo Clinic College of Medicine, Rochester, MN, (4)electronic Child Health Network, Toronto, ON, Canada, (5)Centers for Disease Control and Prevention (CDC), Atlanta, GA, (6)National Library of Medicine, National Institutes of Health, Bethesda, MD, (7)Maternal and Child Health Bureau, Rockville, MD, (8)Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH, HHS, Rockville, MD, (9)Health Resources and Services Administration, HHS, Rockville, MD, (10)National Library of Medicine, National Institutes of Health, HHS, Bethesda, MD