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Effectiveness of 12-13-week scan for early diagnosis of fetal congenital anomalies in the cell-free DNA era.
Kenkhuis, M J A; Bakker, M; Bardi, F; Fontanella, F; Bakker, M K; Fleurke-Rozema, J H; Bilardo, C M.
Afiliação
  • Kenkhuis MJA; Fetal Medicine Unit, Department of Obstetrics & Gynecology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Bakker M; Fetal Medicine Unit, Department of Obstetrics & Gynecology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Bardi F; Fetal Medicine Unit, Department of Obstetrics & Gynecology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Fontanella F; Fetal Medicine Unit, Department of Obstetrics & Gynecology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Bakker MK; Fetal Medicine Unit, Department of Obstetrics & Gynecology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Fleurke-Rozema JH; Eurocat Northern Netherlands, Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Bilardo CM; Fetal Medicine Unit, Department of Obstetrics & Gynecology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Ultrasound Obstet Gynecol ; 51(4): 463-469, 2018 Apr.
Article em En | MEDLINE | ID: mdl-28397377

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Trissomia / Medição da Translucência Nucal / Testes para Triagem do Soro Materno Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Trissomia / Medição da Translucência Nucal / Testes para Triagem do Soro Materno Idioma: En Ano de publicação: 2018 Tipo de documento: Article