P408: Perspectives of rare disease experts on sequencing newborns for treatable genetic conditions*
Nidhi Shah, Robert C. Green(Boston University), Vijay G. Sankaran(Broad Institute), Sophia Adelson(Brigham and Women's Hospital), Rebecca Ganetzky(Children's Hospital of Philadelphia), Shardae Williams(Brigham and Women's Hospital), Jay R. Thiagarajah(University of California, San Francisco), Jason Comander(Massachusetts Eye and Ear Infirmary), Melissa Walker(Massachusetts General Hospital), Ottavia M. Delmonte(National Institutes of Health), Junne Kamihara(Harvard University), Alanna Strong(Children's Hospital of Philadelphia), Nina B. Gold(Harvard University), Jessica A. Gold(Washington University in St. Louis), Amy E. Roberts(Boston Children's Hospital), Alexander M. Holtz(Boston Children's Hospital), Emily Place(MACOM (United States)), Sarah K. Bick(Vanderbilt University), Janey L. Wiggs(Broad Institute), Weizhen Tan(Boston Children's Hospital), Ingrid A. Holm(Boston Children's Hospital)
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