Your browser doesn't support javascript.
loading
Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability.
Monroe, Glen R; Frederix, Gerardus W; Savelberg, Sanne M C; de Vries, Tamar I; Duran, Karen J; van der Smagt, Jasper J; Terhal, Paulien A; van Hasselt, Peter M; Kroes, Hester Y; Verhoeven-Duif, Nanda M; Nijman, Isaäc J; Carbo, Ellen C; van Gassen, Koen L; Knoers, Nine V; Hövels, Anke M; van Haelst, Mieke M; Visser, Gepke; van Haaften, Gijs.
Afiliação
  • Monroe GR; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Frederix GW; Center for Molecular Medicine, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Savelberg SM; Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands.
  • de Vries TI; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Duran KJ; Center for Molecular Medicine, Utrecht University Medical Center, Utrecht, The Netherlands.
  • van der Smagt JJ; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Terhal PA; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • van Hasselt PM; Center for Molecular Medicine, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Kroes HY; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Verhoeven-Duif NM; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Nijman IJ; Department of Metabolic Diseases, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
  • Carbo EC; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • van Gassen KL; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Knoers NV; Center for Molecular Medicine, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Hövels AM; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • van Haelst MM; Center for Molecular Medicine, Utrecht University Medical Center, Utrecht, The Netherlands.
  • Visser G; Department of Genetics, Utrecht University Medical Center, Utrecht, The Netherlands.
  • van Haaften G; Center for Molecular Medicine, Utrecht University Medical Center, Utrecht, The Netherlands.
Genet Med ; 18(9): 949-56, 2016 09.
Article em En | MEDLINE | ID: mdl-26845106
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Sequenciamento de Nucleotídeos em Larga Escala / Sequenciamento do Exoma / Deficiência Intelectual Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Sequenciamento de Nucleotídeos em Larga Escala / Sequenciamento do Exoma / Deficiência Intelectual Idioma: En Ano de publicação: 2016 Tipo de documento: Article