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Familial Klippel–Feil anomaly and t(5;8)(q35.1;p21.1) translocation

2006; Wiley; Volume: 140A; Issue: 9 Linguagem: Inglês

10.1002/ajmg.a.31198

1552-4833

Masahiro Goto, Gen Nishimura, Toshiro Nagai, Kazuki Yamazawa, Tsutomu Ogata,

Congenital Anomalies and Fetal Surgery

American Journal of Medical Genetics Part AVolume 140A, Issue 9 p. 1013-1015 Research Letter Familial Klippel–Feil anomaly and t(5;8)(q35.1;p21.1) translocation† Masahiro Goto, Masahiro Goto Department of Pediatrics, Tokyo Metropolitan Hachioji Children's Hospital, Hachioji, JapanSearch for more papers by this authorGen Nishimura, Gen Nishimura Division of Radiology, Tokyo Metropolitan Kiyose Children's Hospital, Kiyose, JapanSearch for more papers by this authorToshiro Nagai, Toshiro Nagai Department of Pediatrics, Dokkyo University School of Medicine Koshigaya Hospital, Koshigaya, JapanSearch for more papers by this authorKazuki Yamazawa, Kazuki Yamazawa Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, JapanSearch for more papers by this authorTsutomu Ogata, Corresponding Author Tsutomu Ogata [email protected] Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, JapanDepartment of Endocrinology and Metabolism, National Research Institute for Child Health and Development 2-10-1 Ohkura, Setagaya, Tokyo 157-8535, Japan.Search for more papers by this author Masahiro Goto, Masahiro Goto Department of Pediatrics, Tokyo Metropolitan Hachioji Children's Hospital, Hachioji, JapanSearch for more papers by this authorGen Nishimura, Gen Nishimura Division of Radiology, Tokyo Metropolitan Kiyose Children's Hospital, Kiyose, JapanSearch for more papers by this authorToshiro Nagai, Toshiro Nagai Department of Pediatrics, Dokkyo University School of Medicine Koshigaya Hospital, Koshigaya, JapanSearch for more papers by this authorKazuki Yamazawa, Kazuki Yamazawa Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, JapanSearch for more papers by this authorTsutomu Ogata, Corresponding Author Tsutomu Ogata [email protected] Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, JapanDepartment of Endocrinology and Metabolism, National Research Institute for Child Health and Development 2-10-1 Ohkura, Setagaya, Tokyo 157-8535, Japan.Search for more papers by this author First published: 14 April 2006 https://doi.org/10.1002/ajmg.a.31198Citations: 14 † How to cite this article: Goto M, Nishimura G, Nagai T, Yamazawa K, Ogata T. 2006. Familial Klippel–Feil anomaly and t(5;8)(q35.1;p21.1) translocation. Am J Med Genet Part A 140A:1013–1015. 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 Volume140A, Issue91 May 2006Pages 1013-1015 RelatedInformation