Abstract
American Journal of Medical Genetics Part AVolume 143A, Issue 11 p. 1249-1252 Research Letter Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations† Kristin Becker, Corresponding Author Kristin Becker Kristin.Becker@cd-tr.wales.nhs.uk North Wales Clinical Genetics Service, Glan Clwyd Hospital, Rhyl, UK Institute of Medical Genetics, University Hospital of Wales, Cardiff, UKNorth Wales Clinical Genetics Service, Block 12, Glan Clwyd Hospital, Bodelwyddan, Rhyl, Denbighshire LL18 5UJ, UK.Search for more papers by this authorHelen Hughes, Helen Hughes North Wales Clinical Genetics Service, Glan Clwyd Hospital, Rhyl, UK Institute of Medical Genetics, University Hospital of Wales, Cardiff, UKSearch for more papers by this authorKarol Howard, Karol Howard North Wales Clinical Genetics Service, Glan Clwyd Hospital, Rhyl, UKSearch for more papers by this authorMaggie Armstrong, Maggie Armstrong Department of Obstetrics and Gynaecology, Glan Clwyd Hospital, Rhyl, UKSearch for more papers by this authorDevender Roberts, Devender Roberts Fetal Centre, Liverpool Women's Hospital, Liverpool, UKSearch for more papers by this authorEdgar J. Lazda, Edgar J. Lazda Institute of Medical Genetics, University Hospital of Wales, Cardiff, UKSearch for more papers by this authorJohn P. Short, John P. Short Department of Medical Genetics, St. George's Hospital Medical School, London, UKSearch for more papers by this authorAdam Shaw, Adam Shaw Department of Medical Genetics, St. George's Hospital Medical School, London, UKSearch for more papers by this authorMichael A. Patton, Michael A. Patton Department of Medical Genetics, St. George's Hospital Medical School, London, UKSearch for more papers by this authorMarco Tartaglia, Marco Tartaglia Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Rome, ItalySearch for more papers by this author Kristin Becker, Corresponding Author Kristin Becker Kristin.Becker@cd-tr.wales.nhs.uk North Wales Clinical Genetics Service, Glan Clwyd Hospital, Rhyl, UK Institute of Medical Genetics, University Hospital of Wales, Cardiff, UKNorth Wales Clinical Genetics Service, Block 12, Glan Clwyd Hospital, Bodelwyddan, Rhyl, Denbighshire LL18 5UJ, UK.Search for more papers by this authorHelen Hughes, Helen Hughes North Wales Clinical Genetics Service, Glan Clwyd Hospital, Rhyl, UK Institute of Medical Genetics, University Hospital of Wales, Cardiff, UKSearch for more papers by this authorKarol Howard, Karol Howard North Wales Clinical Genetics Service, Glan Clwyd Hospital, Rhyl, UKSearch for more papers by this authorMaggie Armstrong, Maggie Armstrong Department of Obstetrics and Gynaecology, Glan Clwyd Hospital, Rhyl, UKSearch for more papers by this authorDevender Roberts, Devender Roberts Fetal Centre, Liverpool Women's Hospital, Liverpool, UKSearch for more papers by this authorEdgar J. Lazda, Edgar J. Lazda Institute of Medical Genetics, University Hospital of Wales, Cardiff, UKSearch for more papers by this authorJohn P. Short, John P. Short Department of Medical Genetics, St. George's Hospital Medical School, London, UKSearch for more papers by this authorAdam Shaw, Adam Shaw Department of Medical Genetics, St. George's Hospital Medical School, London, UKSearch for more papers by this authorMichael A. Patton, Michael A. Patton Department of Medical Genetics, St. George's Hospital Medical School, London, UKSearch for more papers by this authorMarco Tartaglia, Marco Tartaglia Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Rome, ItalySearch for more papers by this author First published: 11 May 2007 https://doi.org/10.1002/ajmg.a.31738Citations: 8 † How to cite this article: Becker K, Hughes H, Howard K, Armstrong M, Roberts D, Lazda EJ, Short JP, Shaw A, Patton MA, Tartaglia M. 2007. Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations. Am J Med Genet Part A 143A:1249–1252. Read the full textAboutPDF 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 onFacebookTwitterLinked InRedditWechat Citing Literature Volume143A, Issue111 June 2007Pages 1249-1252 RelatedInformation
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