Your browser doesn't support javascript.
loading
Plain-language medical vocabulary for precision diagnosis.
Vasilevsky, Nicole A; Foster, Erin D; Engelstad, Mark E; Carmody, Leigh; Might, Matt; Chambers, Chip; Dawkins, Hugh J S; Lewis, Janine; Della Rocca, Maria G; Snyder, Michelle; Boerkoel, Cornelius F; Rath, Ana; Terry, Sharon F; Kent, Alastair; Searle, Beverly; Baynam, Gareth; Jones, Erik; Gavin, Pam; Bamshad, Michael; Chong, Jessica; Groza, Tudor; Adams, David; Resnick, Adam C; Heath, Allison P; Mungall, Chris; Holm, Ingrid A; Rageth, Kayli; Brownstein, Catherine A; Shefchek, Kent; McMurry, Julie A; Robinson, Peter N; Köhler, Sebastian; Haendel, Melissa A.
Affiliation
  • Vasilevsky NA; Oregon Clinical & Translational Research Institute, Oregon Health & Science University, Portland, OR, USA.
  • Foster ED; Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, OR, USA.
  • Engelstad ME; School of Dentistry, Oregon Health & Science University, Portland, OR, USA.
  • Carmody L; School of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Might M; Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
  • Chambers C; Undiagnosed Disease Network, Boston, MA, USA.
  • Dawkins HJS; School of Medicine, Vanderbilt University, Nashville, TN, USA.
  • Lewis J; Department of Health, Government of Western Australia, Perth, Western Australia, Australia.
  • Della Rocca MG; National Center for Advancing Translational Sciences, Genetic and Rare Diseases Information Center, Bethesda, MD, USA.
  • Snyder M; National Center for Advancing Translational Sciences, Genetic and Rare Diseases Information Center, Bethesda, MD, USA.
  • Boerkoel CF; National Center for Advancing Translational Sciences, Genetic and Rare Diseases Information Center, Bethesda, MD, USA.
  • Rath A; Sanford Health Imagenetics, Sioux Falls, SD, USA.
  • Terry SF; Orphanet, Paris, France.
  • Kent A; Genetic Alliance, Washington, DC, USA.
  • Searle B; Genetic Alliance UK, London, UK.
  • Baynam G; Unique, Oxted, UK.
  • Jones E; Medical School, University of Western Australia, Perth, Western Australia, Australia.
  • Gavin P; Inspire, Arlington, VA, USA.
  • Bamshad M; National Organization for Rare Disorders, Quincy, MA, USA.
  • Chong J; Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Groza T; Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Adams D; Kinghorn Centre for Clinical Genomics, Garvan Institute, Sydney, New South Wales, Australia.
  • Resnick AC; Undiagnosed Disease Program, Bethesda, MD, USA.
  • Heath AP; Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Mungall C; Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Holm IA; Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Rageth K; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Brownstein CA; Sanford Health Imagenetics, Sioux Falls, SD, USA.
  • Shefchek K; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • McMurry JA; Oregon Clinical & Translational Research Institute, Oregon Health & Science University, Portland, OR, USA.
  • Robinson PN; Oregon Clinical & Translational Research Institute, Oregon Health & Science University, Portland, OR, USA.
  • Köhler S; Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
  • Haendel MA; NeuroCure Cluster of Excellence, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Nat Genet ; 50(4): 474-476, 2018 04.
Article de En | MEDLINE | ID: mdl-29632381
Sujet(s)
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Vocabulaire / Médecine de précision / Langage Type d'étude: Diagnostic_studies Aspects: Patient_preference Limites: Humans Langue: En Journal: Nat Genet Sujet du journal: GENETICA MEDICA Année: 2018 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Vocabulaire / Médecine de précision / Langage Type d'étude: Diagnostic_studies Aspects: Patient_preference Limites: Humans Langue: En Journal: Nat Genet Sujet du journal: GENETICA MEDICA Année: 2018 Type de document: Article Pays d'affiliation: États-Unis d'Amérique