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A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.
Corsten-Janssen, Nicole; Bouman, Katelijne; Diphoorn, Janouk C D; Scheper, Arjen J; Kinds, Rianne; El Mecky, Julia; Breet, Hanna; Verheij, Joke B G M; Suijkerbuijk, Ron; Duin, Leonie K; Manten, Gwendolyn T R; van Langen, Irene M; Sijmons, Rolf H; Sikkema-Raddatz, Birgit; Westers, Helga; van Diemen, Cleo C.
Afiliación
  • Corsten-Janssen N; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Bouman K; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Diphoorn JCD; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Scheper AJ; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Kinds R; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • El Mecky J; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Breet H; Clinical Ethics and Law, University of Southampton, Southampton, UK.
  • Verheij JBGM; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Suijkerbuijk R; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Duin LK; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Manten GTR; Department of Obstetrics, Gynecology and Prenatal Diagnosis, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • van Langen IM; Department of Obstetrics and Gynecology, Isala, Zwolle, The Netherlands.
  • Sijmons RH; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Sikkema-Raddatz B; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Westers H; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • van Diemen CC; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Prenat Diagn ; 40(10): 1300-1309, 2020 09.
Article en En | MEDLINE | ID: mdl-32627857
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Anomalías Múltiples / Secuenciación del Exoma Tipo de estudio: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Prenat Diagn Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Anomalías Múltiples / Secuenciación del Exoma Tipo de estudio: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Prenat Diagn Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos