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Kidney abnormalities in persons with monosomy 15q26

2008; Wiley; Volume: 146A; Issue: 13 Linguagem: Inglês

10.1002/ajmg.a.32333

1552-4833

Iosif W. Lurie,

Congenital heart defects research

American Journal of Medical Genetics Part AVolume 146A, Issue 13 p. 1761-1764 Research Letter Kidney abnormalities in persons with monosomy 15q26† Iosif W. Lurie, Corresponding Author Iosif W. Lurie [email protected] Maryland Physicians Associates, Baltimore, Maryland913 Rachel Jordan Court, Owings Mills, MD 21117.Search for more papers by this author Iosif W. Lurie, Corresponding Author Iosif W. Lurie [email protected] Maryland Physicians Associates, Baltimore, Maryland913 Rachel Jordan Court, Owings Mills, MD 21117.Search for more papers by this author First published: 29 May 2008 https://doi.org/10.1002/ajmg.a.32333Citations: 2 † How to cite this article: Lurie IW. 2008. Kidney abnormalities in persons with monosomy 15q26. Am J Med Genet Part A 146A:1761–1764. 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 Adeyinka A, Adams SA, Lorentz CP, van Dyke DL, Jalal SM. 2005. Subtelomere deletions and translocations are frequently familial. Am J Med Genet Part A 135A: 28–35. Bell S, Maclean R, Lozzio CB. 1983. Partial trisomy 3p syndrome due to unbalanced segregation of reciprocal translocations 2/3 and 3/15. Am J Hum Genet 35: 125A. Berg C, Knüpfel M, Geipel A, Kohl T, Krapp M, Knöpfle G, Germer U, Hansmann M, Gembruch U. 2006. 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