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The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.
Srebniak, Malgorzata I; Knapen, Maarten F C M; Polak, Marike; Joosten, Marieke; Diderich, Karin E M; Govaerts, Lutgarde C P; Boter, Marjan; Kromosoeto, Joan N R; van Hassel, Daniella Aloysia C M; Huijbregts, Gido; van IJcken, Wilfred F J; Heydanus, Roger; Dijkman, Anneke; Toolenaar, Toon; de Vries, Femke A T; Knijnenburg, Jeroen; Go, Attie T J I; Galjaard, Robert-Jan H; Van Opstal, Diane.
Afiliação
  • Srebniak MI; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Knapen MFCM; Department of Obstetrics and Gynecology, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Polak M; Foundation Prenatal Screening Southwest region of the Netherlands, Rotterdam, The Netherlands.
  • Joosten M; Institute of Psychology, Erasmus University Rotterdam, Rotterdam, The Netherlands.
  • Diderich KEM; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Govaerts LCP; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Boter M; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Kromosoeto JNR; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • van Hassel DACM; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Huijbregts G; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • van IJcken WFJ; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Heydanus R; Center for Biomics, Erasmus MC, Rotterdam, The Netherlands.
  • Dijkman A; Department of Obstetrics and Gynecology, Amphia Hospital, Breda, The Netherlands.
  • Toolenaar T; Department of Obstetrics and Gynecology, Reinier de Graaf Gasthuis, Delft, The Netherlands.
  • de Vries FAT; Department of Gynecology, Albert Schweitzer Hospital Dordrecht, Dordrecht, The Netherlands.
  • Knijnenburg J; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Go ATJI; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Galjaard RH; Department of Obstetrics and Gynecology, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Van Opstal D; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
Hum Mutat ; 38(7): 880-888, 2017 07.
Article em En | MEDLINE | ID: mdl-28409863
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Ultrassonografia Pré-Natal / Cromossomos / Análise de Sequência com Séries de Oligonucleotídeos / Polimorfismo de Nucleotídeo Único Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Hum Mutat Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Ultrassonografia Pré-Natal / Cromossomos / Análise de Sequência com Séries de Oligonucleotídeos / Polimorfismo de Nucleotídeo Único Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Hum Mutat Ano de publicação: 2017 Tipo de documento: Article