Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes

A. C. Houweling*, Y. M. De Mooij, I. Van Der Burgt, H. G. Yntema, A. M.A. Lachmeijer, A. T.J.I. Go

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)284-286
Number of pages3
JournalPrenatal Diagnosis
Volume30
Issue number3
DOIs
Publication statusPublished - Mar 2010
Externally publishedYes

Keywords

  • KRAS
  • Noonan syndrome
  • Nuchal translucency
  • Prenatal
  • PTPN11

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