Your browser doesn't support javascript.
loading
The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children.
Freed, Amanda S; Clowes Candadai, Sarah V; Sikes, Megan C; Thies, Jenny; Byers, Heather M; Dines, Jennifer N; Ndugga-Kabuye, Mesaki Kenneth; Smith, Mallory B; Fogus, Katie; Mefford, Heather C; Lam, Christina; Adam, Margaret P; Sun, Angela; McGuire, John K; DiGeronimo, Robert; Dipple, Katrina M; Deutsch, Gail H; Billimoria, Zeenia C; Bennett, James T.
Afiliación
  • Freed AS; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA.
  • Clowes Candadai SV; Department of Laboratories, Seattle Children's Hospital, Seattle, WA; Patient-centered Laboratory Utilization Guidance Services (PLUGS), Seattle Children's Hospital, Seattle, WA.
  • Sikes MC; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA.
  • Thies J; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA.
  • Byers HM; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA.
  • Dines JN; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA.
  • Ndugga-Kabuye MK; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA.
  • Smith MB; Division of Pediatric Critical Care, Department of Pediatrics, University of Washington, Seattle, WA.
  • Fogus K; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA.
  • Mefford HC; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA; Brotman Baty Institute for Precision Medicine, Seattle, WA.
  • Lam C; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA; Brotman Baty Institute for Precision Medicine, Seattle, WA; Center for Integrative Brain Research, Seattle Children's Research Instit
  • Adam MP; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA.
  • Sun A; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA.
  • McGuire JK; Division of Pediatric Critical Care, Department of Pediatrics, University of Washington, Seattle, WA.
  • DiGeronimo R; Division of Neonatology, Department of Pediatrics, University of Washington, Seattle, WA.
  • Dipple KM; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA; Center for Clinical and Translational Research, Seattle Children's Research Institute, Seattle, WA.
  • Deutsch GH; Department of Pathology, University of Washington and Seattle Children's Hospital, Seattle, WA.
  • Billimoria ZC; Division of Neonatology, Department of Pediatrics, University of Washington, Seattle, WA.
  • Bennett JT; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA; Brotman Baty Institute for Precision Medicine, Seattle, WA; Center for Developmental Biology and Regenerative Medicine, Seattle Child
J Pediatr ; 226: 202-212.e1, 2020 11.
Article en En | MEDLINE | ID: mdl-32553838
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Secuenciación del Exoma / Enfermedades Genéticas Congénitas Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Pediatr Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Secuenciación del Exoma / Enfermedades Genéticas Congénitas Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Pediatr Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos