An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm

Author:

Dimmock David P.,Clark Michelle M.,Gaughran Mary,Cakici Julie A.,Caylor Sara A.,Clarke Christina,Feddock Michele,Chowdhury Shimul,Salz Lisa,Cheung Cynthia,Bird Lynne M.,Hobbs Charlotte,Wigby Kristen,Farnaes Lauge,Bloss Cinnamon S.,Kingsmore Stephen F.ORCID,Bainbridge Matthew N.,Barea Jaime,Batalov Sergey,Bezares Zaira,Bird Lynne M.,Bloss Cinnamon S.,Braun Joshua J.A.,Cakici Julie A.,Del Campo Miguel,Carroll Jeanne,Cheung Cynthia,Cohenmeyer Casey,Coufal Nicole G.,Diaz Carlos,Ding Yan,Ellsworth Katarzyna,Evans Marva,Feigenbaum Annette,Friedman Jennifer,Gleeson Joe,Hansen Christian,Honold Jose,James Kiely,Jones Marilyn C.,Kimball Amy,Knight Gail,Van Der Kraan Lucitia,Lane Brian,Le Jennie,Leibel Sandra,Lenberg Jerica,Mashburn Dana,Moyer Laurel,Mulrooney Patrick,Nahas Shareef,Oh Daeheon,Orendain Daniken,Oriol Albert,Ortiz-Arechiga Maria,Prince Lance,Rego Seema,Reyes Iris,Sanford Erica,Sauer Charles,Schwanemann Leila,Speziale Mark,Suttner Denise,Sweeney Nathaly,Song Richard,Tokita Mari,Veeraraghavan Narayanan,Watkins Kelly,Wong Terence,Wright Meredith S.,Yamada Catherine

Funder

National Human Genome Research Institute

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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