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Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU.
Sanford, Erica F; Clark, Michelle M; Farnaes, Lauge; Williams, Matthew R; Perry, James C; Ingulli, Elizabeth G; Sweeney, Nathaly M; Doshi, Ami; Gold, Jeffrey J; Briggs, Benjamin; Bainbridge, Matthew N; Feddock, Michele; Watkins, Kelly; Chowdhury, Shimul; Nahas, Shareef A; Dimmock, David P; Kingsmore, Stephen F; Coufal, Nicole G.
Afiliación
  • Sanford EF; Department of Pediatrics, University of California at San Diego, La Jolla, CA.
  • Clark MM; Rady Children's Hospital San Diego, San Diego, CA.
  • Farnaes L; Rady Children's Institute for Genomic Medicine, San Diego, CA.
  • Williams MR; Rady Children's Institute for Genomic Medicine, San Diego, CA.
  • Perry JC; Rady Children's Institute for Genomic Medicine, San Diego, CA.
  • Ingulli EG; Department of Pediatrics, University of California at San Diego, La Jolla, CA.
  • Sweeney NM; Rady Children's Hospital San Diego, San Diego, CA.
  • Doshi A; Department of Pediatrics, University of California at San Diego, La Jolla, CA.
  • Gold JJ; Rady Children's Hospital San Diego, San Diego, CA.
  • Briggs B; Rady Children's Hospital San Diego, San Diego, CA.
  • Bainbridge MN; Rady Children's Hospital San Diego, San Diego, CA.
  • Feddock M; Rady Children's Institute for Genomic Medicine, San Diego, CA.
  • Watkins K; Rady Children's Hospital San Diego, San Diego, CA.
  • Chowdhury S; Rady Children's Hospital San Diego, San Diego, CA.
  • Nahas SA; Department of Neuroscience, University of California at San Diego, La Jolla, CA.
  • Dimmock DP; Department of Pediatrics, University of California at San Diego, La Jolla, CA.
  • Kingsmore SF; Rady Children's Hospital San Diego, San Diego, CA.
  • Coufal NG; Rady Children's Institute for Genomic Medicine, San Diego, CA.
Pediatr Crit Care Med ; 20(11): 1007-1020, 2019 11.
Article en En | MEDLINE | ID: mdl-31246743
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Secuenciación Completa del Genoma / Enfermedades Genéticas Congénitas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Pediatr Crit Care Med Asunto de la revista: PEDIATRIA / TERAPIA INTENSIVA Año: 2019 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Secuenciación Completa del Genoma / Enfermedades Genéticas Congénitas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Pediatr Crit Care Med Asunto de la revista: PEDIATRIA / TERAPIA INTENSIVA Año: 2019 Tipo del documento: Article