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Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Hart, M Ragan; Biesecker, Barbara B; Blout, Carrie L; Christensen, Kurt D; Amendola, Laura M; Bergstrom, Katie L; Biswas, Sawona; Bowling, Kevin M; Brothers, Kyle B; Conlin, Laura K; Cooper, Greg M; Dulik, Matthew C; East, Kelly M; Everett, Jessica N; Finnila, Candice R; Ghazani, Arezou A; Gilmore, Marian J; Goddard, Katrina A B; Jarvik, Gail P; Johnston, Jennifer J; Kauffman, Tia L; Kelley, Whitley V; Krier, Joel B; Lewis, Katie L; McGuire, Amy L; McMullen, Carmit; Ou, Jeffrey; Plon, Sharon E; Rehm, Heidi L; Richards, C Sue; Romasko, Edward J; Sagardia, Ane Miren; Spinner, Nancy B; Thompson, Michelle L; Turbitt, Erin; Vassy, Jason L; Wilfond, Benjamin S; Veenstra, David L; Berg, Jonathan S; Green, Robert C; Biesecker, Leslie G; Hindorff, Lucia A.
Affiliation
  • Hart MR; Department of Medicine (Medical Genetics), University of Washington, Seattle, WA, USA. hartmr@uw.edu.
  • Biesecker BB; Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA. hartmr@uw.edu.
  • Blout CL; Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
  • Christensen KD; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Amendola LM; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Bergstrom KL; Harvard Medical School, Boston, MA, USA.
  • Biswas S; Department of Medicine (Medical Genetics), University of Washington, Seattle, WA, USA.
  • Bowling KM; Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA.
  • Brothers KB; Department of Pediatrics, Oncology Section, Baylor College of Medicine, Houston, TX, USA.
  • Conlin LK; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Cooper GM; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
  • Dulik MC; Department of Pediatrics, University of Louisville, Louisville, KY, USA.
  • East KM; Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital, Philadelphia, PA, USA.
  • Everett JN; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Finnila CR; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
  • Ghazani AA; Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital, Philadelphia, PA, USA.
  • Gilmore MJ; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Goddard KAB; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
  • Jarvik GP; Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
  • Johnston JJ; Michigan Center for Translational Pathology, University of Michigan, Ann Arbor, MI, USA.
  • Kauffman TL; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
  • Kelley WV; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Krier JB; Department of Medical Genetics, Kaiser Permanente Northwest, Portland, OR, USA.
  • Lewis KL; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • McGuire AL; Department of Medicine (Medical Genetics), University of Washington, Seattle, WA, USA.
  • McMullen C; Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA.
  • Ou J; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
  • Plon SE; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Rehm HL; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
  • Richards CS; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Romasko EJ; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
  • Sagardia AM; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX, USA.
  • Spinner NB; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Thompson ML; Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA.
  • Turbitt E; Department of Pediatrics, Oncology Section, Baylor College of Medicine, Houston, TX, USA.
  • Vassy JL; Harvard Medical School, Boston, MA, USA.
  • Wilfond BS; Laboratory for Molecular Medicine, Partners HealthCare, Cambridge, MA, USA.
  • Veenstra DL; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Berg JS; Knight Diagnostic Laboratories, Oregon Health Science University, Portland, OR, USA.
  • Green RC; Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital, Philadelphia, PA, USA.
  • Biesecker LG; Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
  • Hindorff LA; Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital, Philadelphia, PA, USA.
Genet Med ; 21(5): 1261-1262, 2019 May.
Article in En | MEDLINE | ID: mdl-30670880
The originally published version of this Article contained errors in Fig. 2. The numbers below the black arrowheads were incorrect; please see incorrect Figure in associated Correction. These errors have now been corrected in the PDF and HTML versions of the Article.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Health_economic_evaluation / Prevalence_studies / Risk_factors_studies Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2019 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Health_economic_evaluation / Prevalence_studies / Risk_factors_studies Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2019 Document type: Article Affiliation country: Country of publication: