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• W2016335024 abstract "American Journal of Medical Genetics Part AVolume 158A, Issue 7 p. 1788-1792 Research Letter Duplication of 18q21.32–q22.3 identified in a stillborn and two relatives with minimal dysmorphic features† Kaylee E. Henson, Corresponding Author Kaylee E. Henson khenson@ecommunity.com Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaMaternal Fetal Medicine, Community Health Network, 7120 Clearvista Dr., Suite 5900, Indianapolis, IN 46256.Search for more papers by this authorKarrie A. Hines, Karrie A. Hines Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorDavid D. Weaver, David D. Weaver Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorWilfredo M. Torres, Wilfredo M. Torres Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorJennifer Verbrugge, Jennifer Verbrugge Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorKristyne Stone, Kristyne Stone Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorGail H. Vance, Gail H. Vance Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this author Kaylee E. Henson, Corresponding Author Kaylee E. Henson khenson@ecommunity.com Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaMaternal Fetal Medicine, Community Health Network, 7120 Clearvista Dr., Suite 5900, Indianapolis, IN 46256.Search for more papers by this authorKarrie A. Hines, Karrie A. Hines Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorDavid D. Weaver, David D. Weaver Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorWilfredo M. Torres, Wilfredo M. Torres Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorJennifer Verbrugge, Jennifer Verbrugge Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorKristyne Stone, Kristyne Stone Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this authorGail H. Vance, Gail H. Vance Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IndianaSearch for more papers by this author First published: 31 May 2012 https://doi.org/10.1002/ajmg.a.35405Citations: 4 † How to Cite this Article: Henson KE, Hines KA, Weaver DD, Torres WM, Verbrugge J, Stone K, Vance GH. 2012. Duplication of 18q21.32–q22.3 identified in a stillborn and two relatives with minimal dysmorphic features. Am J Med Genet Part A. 158A:1788–1792. 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 Volume158A, Issue7July 2012Pages 1788-1792 RelatedInformation" @default.
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