Title: A girl with Down syndrome and partial trisomy for 21pter‐q22.13: A clue to narrow the Down syndrome critical region
Abstract: American Journal of Medical Genetics Part AVolume 146A, Issue 1 p. 124-127 Research Letter A girl with Down syndrome and partial trisomy for 21pter-q22.13: A clue to narrow the Down syndrome critical region† Daisuke Sato, Daisuke Sato Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, JapanSearch for more papers by this authorHiroki Kawara, Hiroki Kawara Kyushu Medical Science, Nagasaki, JapanSearch for more papers by this authorOsamu Shimokawa, Osamu Shimokawa Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, Japan Kyushu Medical Science, Nagasaki, JapanSearch for more papers by this authorNaoki Harada, Naoki Harada Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, Japan Kyushu Medical Science, Nagasaki, JapanSearch for more papers by this authorHidefumi Tonoki, Hidefumi Tonoki Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan Department of Pediatrics, Caress Alliance Medical Corporation, Tenshi Hospital, Sapporo, Japan Section of Clinical Genetics, Caress Alliance Medical Corporation, Sapporo, JapanSearch for more papers by this authorNobuhiro Takahashi, Nobuhiro Takahashi Department of Pediatrics, Caress Alliance Medical Corporation, Tenshi Hospital, Sapporo, JapanSearch for more papers by this authorYumi Imai, Yumi Imai Section of Clinical Genetics, Caress Alliance Medical Corporation, Sapporo, JapanSearch for more papers by this authorHiromi Kimura, Hiromi Kimura Section of Clinical Genetics, Caress Alliance Medical Corporation, Sapporo, JapanSearch for more papers by this authorNaomichi Matsumoto, Naomichi Matsumoto Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, Japan Department of Human Genetics, Yokohama City Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorTadashi Ariga, Tadashi Ariga Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, JapanSearch for more papers by this authorNorio Niikawa, Norio Niikawa Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, JapanSearch for more papers by this authorKoh-ichiro Yoshiura, Corresponding Author Koh-ichiro Yoshiura [email protected] Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, JapanDepartment of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Sakamoto 1-12-4, Nagasaki 852-8523, Japan.Search for more papers by this author Daisuke Sato, Daisuke Sato Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, JapanSearch for more papers by this authorHiroki Kawara, Hiroki Kawara Kyushu Medical Science, Nagasaki, JapanSearch for more papers by this authorOsamu Shimokawa, Osamu Shimokawa Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, Japan Kyushu Medical Science, Nagasaki, JapanSearch for more papers by this authorNaoki Harada, Naoki Harada Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, Japan Kyushu Medical Science, Nagasaki, JapanSearch for more papers by this authorHidefumi Tonoki, Hidefumi Tonoki Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan Department of Pediatrics, Caress Alliance Medical Corporation, Tenshi Hospital, Sapporo, Japan Section of Clinical Genetics, Caress Alliance Medical Corporation, Sapporo, JapanSearch for more papers by this authorNobuhiro Takahashi, Nobuhiro Takahashi Department of Pediatrics, Caress Alliance Medical Corporation, Tenshi Hospital, Sapporo, JapanSearch for more papers by this authorYumi Imai, Yumi Imai Section of Clinical Genetics, Caress Alliance Medical Corporation, Sapporo, JapanSearch for more papers by this authorHiromi Kimura, Hiromi Kimura Section of Clinical Genetics, Caress Alliance Medical Corporation, Sapporo, JapanSearch for more papers by this authorNaomichi Matsumoto, Naomichi Matsumoto Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, Japan Department of Human Genetics, Yokohama City Graduate School of Medicine, Yokohama, JapanSearch for more papers by this authorTadashi Ariga, Tadashi Ariga Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, JapanSearch for more papers by this authorNorio Niikawa, Norio Niikawa Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, JapanSearch for more papers by this authorKoh-ichiro Yoshiura, Corresponding Author Koh-ichiro Yoshiura [email protected] Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan Solution Oriented Research of Science and Technology (SORST), Japan Science and Technology Agency (JST), Kawaguchi, JapanDepartment of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Sakamoto 1-12-4, Nagasaki 852-8523, Japan.Search for more papers by this author First published: 19 December 2007 https://doi.org/10.1002/ajmg.a.31974Citations: 5 † How to cite this article: Sato D, Kawara H, Shimokawa O, Harada N, Tonoki H, Takahashi N, Imai Y, Kimura H, Matsumoto N, Ariga T, Niikawa N, Yoshiura K. 2007. A girl with Down syndrome and partial trisomy for 21pter-q22.13: A clue to narrow the Down syndrome critical region. Am J Med Genet Part A 146A:124–127. 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 Citing Literature Volume146A, Issue11 January 2008Pages 124-127 RelatedInformation
Publication Year: 2007
Publication Date: 2007-12-19
Language: en
Type: article
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 6
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