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• W2600861898 abstract "American Journal of Medical Genetics Part AVolume 173, Issue 4 p. 1090-1093 Research Letter Novel clinical findings in the first Egyptian case of Sotos syndrome caused by complete deletion of the NSD1 gene Ebtesam Abdalla, Ebtesam Abdalla Faculty of Medicine, Department of Genetic Medicine, King Abdulaziz University, Jeddah, Saudi Arabia Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, EgyptSearch for more papers by this authorOliver Bartsch, Oliver Bartsch Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, GermanySearch for more papers by this authorDanuta Galetzka, Danuta Galetzka Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, GermanySearch for more papers by this authorUlrich Zechner, Corresponding Author Ulrich Zechner ulrich.zechner@unimedizin-mainz.de Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany Correspondence to: Ulrich Zechner, Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131 Mainz, Germany. E-mail: ulrich.zechner@unimedizin-mainz.deSearch for more papers by this author Ebtesam Abdalla, Ebtesam Abdalla Faculty of Medicine, Department of Genetic Medicine, King Abdulaziz University, Jeddah, Saudi Arabia Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, EgyptSearch for more papers by this authorOliver Bartsch, Oliver Bartsch Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, GermanySearch for more papers by this authorDanuta Galetzka, Danuta Galetzka Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, GermanySearch for more papers by this authorUlrich Zechner, Corresponding Author Ulrich Zechner ulrich.zechner@unimedizin-mainz.de Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany Correspondence to: Ulrich Zechner, Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131 Mainz, Germany. E-mail: ulrich.zechner@unimedizin-mainz.deSearch for more papers by this author First published: 22 March 2017 https://doi.org/10.1002/ajmg.a.38107 Conflicts of interest: The authors indicate they have no financial relationships relevant to this article to disclose. The authors declare that they have no competing interests. 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 onFacebookTwitterLinkedInRedditWechat Volume173, Issue4April 2017Pages 1090-1093 RelatedInformation" @default.
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• W2600861898 title "Novel clinical findings in the first Egyptian case of Sotos syndrome caused by complete deletion of the<i>NSD1</i>gene" @default.
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