Interstitial deletion 5q14.3‐q21 associated with iris coloboma, hearing loss, dental anomaly, moderate intellectual disability, and attention deficit and hyperactivity disorder
2009; Wiley; Volume: 149A; Issue: 11 Linguagem: Inglês
10.1002/ajmg.a.33079
ISSN1552-4833
AutoresNara Sobreira, Michael F. Walsh, Denise Batista, Tao Wang,
Tópico(s)Chromosomal and Genetic Variations
ResumoAmerican Journal of Medical Genetics Part AVolume 149A, Issue 11 p. 2581-2583 Research Letter Interstitial deletion 5q14.3-q21 associated with iris coloboma, hearing loss, dental anomaly, moderate intellectual disability, and attention deficit and hyperactivity disorder† Nara Sobreira, Nara Sobreira Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MarylandSearch for more papers by this authorMichael F. Walsh, Michael F. Walsh Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MarylandSearch for more papers by this authorDenise Batista, Denise Batista Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland Kennedy Krieger Institute, Baltimore, MarylandSearch for more papers by this authorTao Wang, Corresponding Author Tao Wang [email protected] Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MarylandMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, 733 North Broadway, BRB513, Baltimore, MD 21205.Search for more papers by this author Nara Sobreira, Nara Sobreira Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MarylandSearch for more papers by this authorMichael F. Walsh, Michael F. Walsh Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MarylandSearch for more papers by this authorDenise Batista, Denise Batista Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland Kennedy Krieger Institute, Baltimore, MarylandSearch for more papers by this authorTao Wang, Corresponding Author Tao Wang [email protected] Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MarylandMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, 733 North Broadway, BRB513, Baltimore, MD 21205.Search for more papers by this author First published: 28 October 2009 https://doi.org/10.1002/ajmg.a.33079Citations: 15 † How to cite this article: Sobreira N, Walsh MF, Batista D, Wang T. 2009. Interstitial deletion 5q14.3-q21 associated with iris coloboma, hearing loss, dental anomaly, moderate intellectual disability, and attention deficit and hyperactivity disorder. Am J Med Genet Part A 149A:2581–2583. 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 onEmailFacebookTwitterLinkedInRedditWechat REFERENCES Baekvad-Hansen M, Tümer Z, Delicado A, Erdogan F, Tommerup N, Larsen LA. 2006. Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease. Am J Med Genet Part A 140A: 427–433. Bloch-Zupan A, Goodman JR. 2006. Otodental syndrome. Orphanet J Rare Dis 1: 5. 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