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

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)284-286
JournalPrenatal Diagnosis
Volume30
Issue number3
DOIs
Publication statusPublished - 2010

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Houweling, A. C., de Mooij, Y. M., van der Burgt, I., Yntema, H. G., Lachmeijer, A. M. A., & Go, A. T. J. I. (2010). Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes. Prenatal Diagnosis, 30(3), 284-286. https://doi.org/10.1002/pd.2458