De novo deletion of 1q24.3-q31.2 in a patient with severe growth retardation
2010; Wiley; Volume: 152A; Issue: 5 Linguagem: Inglês
10.1002/ajmg.a.33371
ISSN1552-4833
AutoresAkira Nishimura, Yoko Hiraki, Hiroko Shimoda, Gen Nishimura, Hiromi Tadaki, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Naomichi Matsumoto,
Tópico(s)Genomic variations and chromosomal abnormalities
ResumoAmerican Journal of Medical Genetics Part AVolume 152A, Issue 5 p. 1322-1325 Research Letter De novo deletion of 1q24.3-q31.2 in a patient with severe growth retardation† Akira Nishimura, Akira Nishimura Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorYoko Hiraki, Yoko Hiraki Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan Hiroshima Municipal Center for Child Health and Development, Hiroshima, JapanSearch for more papers by this authorHiroko Shimoda, Hiroko Shimoda Department of Pediatrics, National Hospital Organization, Higashi-Hiroshima Medical Center, Higashi-Hiroshima, JapanSearch for more papers by this authorGen Nishimura, Gen Nishimura Department of Radiology, Tokyo Metropolitan Kiyose Children's Hospital, Kiyose, JapanSearch for more papers by this authorHiromi Tadaki, Hiromi Tadaki Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorYoshinori Tsurusaki, Yoshinori Tsurusaki Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorNoriko Miyake, Noriko Miyake Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorHirotomo Saitsu, Hirotomo Saitsu Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorNaomichi Matsumoto, Corresponding Author Naomichi Matsumoto naomat@yokohama-cu.ac.jp Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Fukuura 3-9, Kanazawa-ku, Yokohama 236-0004, Japan.Search for more papers by this author Akira Nishimura, Akira Nishimura Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorYoko Hiraki, Yoko Hiraki Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan Hiroshima Municipal Center for Child Health and Development, Hiroshima, JapanSearch for more papers by this authorHiroko Shimoda, Hiroko Shimoda Department of Pediatrics, National Hospital Organization, Higashi-Hiroshima Medical Center, Higashi-Hiroshima, JapanSearch for more papers by this authorGen Nishimura, Gen Nishimura Department of Radiology, Tokyo Metropolitan Kiyose Children's Hospital, Kiyose, JapanSearch for more papers by this authorHiromi Tadaki, Hiromi Tadaki Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorYoshinori Tsurusaki, Yoshinori Tsurusaki Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorNoriko Miyake, Noriko Miyake Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorHirotomo Saitsu, Hirotomo Saitsu Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorNaomichi Matsumoto, Corresponding Author Naomichi Matsumoto naomat@yokohama-cu.ac.jp Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, JapanDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Fukuura 3-9, Kanazawa-ku, Yokohama 236-0004, Japan.Search for more papers by this author First published: 13 April 2010 https://doi.org/10.1002/ajmg.a.33371Citations: 16 † How to cite this article: Nishimura A, Hiraki Y, Shimoda H, Nishimura G, Tadaki H, Tsurusaki Y, Miyake N, Saitsu H, Matsumoto N. 2010. De novo deletion of 1q24.3-q31.2 in a patient with severe growth retardation. Am J Med Genet Part A 152A:1322–1325. 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 Volume152A, Issue5May 2010Pages 1322-1325 RelatedInformation
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