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A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.
Tsiplova, Kate; Zur, Richard M; Marshall, Christian R; Stavropoulos, Dimitri J; Pereira, Sergio L; Merico, Daniele; Young, Edwin J; Sung, Wilson W L; Scherer, Stephen W; Ungar, Wendy J.
Afiliação
  • Tsiplova K; Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Zur RM; Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Marshall CR; Genome Diagnostics, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Stavropoulos DJ; Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
  • Pereira SL; Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
  • Merico D; Cytogenetics, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Young EJ; The Centre for Applied Genomics and Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Sung WWL; The Centre for Applied Genomics and Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Scherer SW; Cytogenetics, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Ungar WJ; The Centre for Applied Genomics and Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Genet Med ; 19(11): 1268-1275, 2017 11.
Article em En | MEDLINE | ID: mdl-28471434
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise em Microsséries / Transtorno do Espectro Autista / Sequenciamento Completo do Genoma / Sequenciamento do Exoma Tipo de estudo: Diagnostic_studies / Health_economic_evaluation Limite: Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise em Microsséries / Transtorno do Espectro Autista / Sequenciamento Completo do Genoma / Sequenciamento do Exoma Tipo de estudo: Diagnostic_studies / Health_economic_evaluation Limite: Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Canadá