Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging

C. Deden, K. Neveling, D. Zafeiropopoulou, C. Gilissen, R. Pfundt, T. Rinne, N. de Leeuw, B. Faas, T. Gardeitchik, S.C.E.H. Sallevelt, A. Paulussen, S.J.C. Stevens, E. Sikkel, M.W. Elting, M.C. van Maarle, K.E.M. Diderich, N. Corsten-Janssen, K.D. Lichtenbelt, G. Lachmeijer, L.E.L.M. VissersH.G. Yntema, M. Nelen, I. Feenstra, W.A.G. van Zelst-Stams

Research output: Contribution to journalArticleAcademicpeer-review

13 Citations (Web of Science)
Original languageEnglish
Pages (from-to)972-983
Number of pages12
JournalPrenatal Diagnosis
Volume40
Issue number8
DOIs
Publication statusPublished - 1 Jul 2020

Keywords

  • abnormalities
  • diagnosis
  • infants
  • microarray
  • utility
  • DIAGNOSIS
  • MICROARRAY
  • ABNORMALITIES
  • INFANTS
  • UTILITY

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