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

Abstract

Prenatal DiagnosisVolume 30, Issue 3 p. 284-286 Research Letter Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes A. C. Houweling, Corresponding Author A. C. Houweling a.houweling@vumc.nl Department of Clinical Genetics and Human Genetics, VU University Medical Center, Amsterdam, The NetherlandsVU Medisch Centrum, Receptie D, Postbus 7057, Amsterdam, The Netherlands.Search for more papers by this authorY. M. de Mooij, Y. M. de Mooij Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam, The NetherlandsSearch for more papers by this authorI. van der Burgt, I. van der Burgt Department of Human Genetics, University Medical Center St Radboud, Nijmegen, The NetherlandsSearch for more papers by this authorH. G. Yntema, H. G. Yntema Department of Human Genetics, University Medical Center St Radboud, Nijmegen, The NetherlandsSearch for more papers by this authorA. M. A. Lachmeijer, A. M. A. Lachmeijer Department of Clinical Genetics and Human Genetics, VU University Medical Center, Amsterdam, The NetherlandsSearch for more papers by this authorA. T. J. I. Go, A. T. J. I. Go Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam, The NetherlandsSearch for more papers by this author A. C. Houweling, Corresponding Author A. C. Houweling a.houweling@vumc.nl Department of Clinical Genetics and Human Genetics, VU University Medical Center, Amsterdam, The NetherlandsVU Medisch Centrum, Receptie D, Postbus 7057, Amsterdam, The Netherlands.Search for more papers by this authorY. M. de Mooij, Y. M. de Mooij Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam, The NetherlandsSearch for more papers by this authorI. van der Burgt, I. van der Burgt Department of Human Genetics, University Medical Center St Radboud, Nijmegen, The NetherlandsSearch for more papers by this authorH. G. Yntema, H. G. Yntema Department of Human Genetics, University Medical Center St Radboud, Nijmegen, The NetherlandsSearch for more papers by this authorA. M. A. Lachmeijer, A. M. A. Lachmeijer Department of Clinical Genetics and Human Genetics, VU University Medical Center, Amsterdam, The NetherlandsSearch for more papers by this authorA. T. J. I. Go, A. T. J. I. Go Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam, The NetherlandsSearch for more papers by this author First published: 28 January 2010 https://doi.org/10.1002/pd.2458Citations: 19AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume30, Issue3March 2010Pages 284-286 RelatedInformation