What's in a name? The 22q11.2 deletion

Abstract

American Journal of Medical GeneticsVolume 72, Issue 2 p. 247-247 Letter to the EditorFree Access What's in a name? The 22q11.2 deletion Donna M. McDonald-McGinn, Corresponding Author Donna M. McDonald-McGinn Division of Human Genetics and Molecular Biology, Philadelphia, PennsylvaniaClinical Genetics Center, The Children's Hospital of Philadelphia, 34th and Civic Center Boulevard, Philadelphia, PA 19104.Search for more papers by this authorElaine H. Zackai, Elaine H. Zackai Division of Human Genetics and Molecular Biology, Philadelphia, PennsylvaniaSearch for more papers by this authorDavid Low, David Low Division of Plastic and Reconstructive, Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania Department of Pediatrics, University of Pennsylvania, School of Medicine, Philadelphia, PennsylvaniaSearch for more papers by this author Donna M. McDonald-McGinn, Corresponding Author Donna M. McDonald-McGinn Division of Human Genetics and Molecular Biology, Philadelphia, PennsylvaniaClinical Genetics Center, The Children's Hospital of Philadelphia, 34th and Civic Center Boulevard, Philadelphia, PA 19104.Search for more papers by this authorElaine H. Zackai, Elaine H. Zackai Division of Human Genetics and Molecular Biology, Philadelphia, PennsylvaniaSearch for more papers by this authorDavid Low, David Low Division of Plastic and Reconstructive, Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania Department of Pediatrics, University of Pennsylvania, School of Medicine, Philadelphia, PennsylvaniaSearch for more papers by this author First published: 06 December 1998 https://doi.org/10.1002/(SICI)1096-8628(19971017)72:2<247::AID-AJMG25>3.0.CO;2-MCitations: 17AboutPDF 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 No abstract is available for this article. References Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J: (1993): Conotruncal anomaly face syndrome is associated with a deletion within 22q11. J Med Genet 30: 822– 824. McDonald-McGinn DM, Zackai EH: (1996): The history of the 22q11.2 deletion. “22q and You,” a newsletter for families and professionals. Summer 1–11. Wilson DI, Burn J, Scambler P, Goodship J: (1993): DiGeorge syndrome: Part of Catch 22. J Med Genet 30: 852– 856. Wulfsberg EA, Leana-Cox J, Neri G: (1996): What's in a name? Chromosome 22q Abnormalities and the DiGeorge, Velocardiofacial, and Conotruncal Anomalies Face syndromes. Am J Med Genet 65: 317– 319. Citing Literature Volume72, Issue217 October 1997Pages 247-247 ReferencesRelatedInformation