Abstract: American Journal of Medical Genetics Part AVolume 135A, Issue 2 p. 224-226 Research Letter OEIS complex with del(3)(q12.2q13.2) Rika Kosaki, Corresponding Author Rika Kosaki [email protected] Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanDepartment of Clinical Genetics and Molecular Medicine, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan.Search for more papers by this authorYasuyuki Fukuhara, Yasuyuki Fukuhara Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorMotomichi Kosuga, Motomichi Kosuga Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorTorayuki Okuyama, Torayuki Okuyama Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorNoriko Kawashima, Noriko Kawashima Department of Surgery, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorToshiro Honna, Toshiro Honna Department of Surgery, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorKatsuhiko Ueoka, Katsuhiko Ueoka Department of Urology, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorKenjiro Kosaki, Kenjiro Kosaki Department of Pediatrics, Keio University School of Medicine, Tokyo, JapanSearch for more papers by this author Rika Kosaki, Corresponding Author Rika Kosaki [email protected] Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanDepartment of Clinical Genetics and Molecular Medicine, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan.Search for more papers by this authorYasuyuki Fukuhara, Yasuyuki Fukuhara Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorMotomichi Kosuga, Motomichi Kosuga Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorTorayuki Okuyama, Torayuki Okuyama Department of Clinical Genetics and Molecular Medicine, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorNoriko Kawashima, Noriko Kawashima Department of Surgery, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorToshiro Honna, Toshiro Honna Department of Surgery, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorKatsuhiko Ueoka, Katsuhiko Ueoka Department of Urology, National Children's Medical Center, Tokyo, JapanSearch for more papers by this authorKenjiro Kosaki, Kenjiro Kosaki Department of Pediatrics, Keio University School of Medicine, Tokyo, JapanSearch for more papers by this author First published: 10 May 2005 https://doi.org/10.1002/ajmg.a.30733Citations: 40Read 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 Arai K, Matukiyo H, Takazawa H. 1982. A case report of partial deletion of the long arm of the no. 3 chromosome. Med Genet Res 4: 1–4. Google Scholar Cai WW, Mao JH, Chow CW, Damani S, Balmain A, Bradley A. 2002. Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays. Nat Biotechnol 20: 393–396. 10.1038/nbt0402-393 CASPubMedWeb of Science®Google Scholar Carey JC, Greenbaum B, Hall BD. 1978. The OEIS complex (omphalocele, exstrophy, imperforate anus, spinal defects). Birth Defects Orig Artic Ser 14: 253–263. CASPubMedGoogle Scholar Genuardi M, Calvieri F, Tozzi C, Coslovi R, Neri G. 1994. A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum. Clin Dysmorphol 3: 292–296. 10.1097/00019605-199410000-00003 CASPubMedGoogle Scholar Jenkins MB, Stang HJ, Davis E, Boyd L. 1985. Deletion of the proximal long arm of chromosome 3 in an infant with features of turner syndrome. Ann Genet 28: 42–44. CASPubMedWeb of Science®Google Scholar Koffler H, Aase JM, Papile LA, Coen RW. 1978. Persistent cloaca with absent penis and anal atresia in one of identical twins. J Pediatr 93: 821–823. 10.1016/S0022-3476(78)81092-0 CASPubMedWeb of Science®Google Scholar McLaughlin JF, Marks WM, Jones G. 1984. Prospective management of exstrophy of the cloaca and myelocystocele following prenatal ultrasound recognition of neural tube defects in identical twins. Am J Med Genet 19: 721–727. 10.1002/ajmg.1320190412 CASPubMedWeb of Science®Google Scholar McMorrow LE, Reid CS, Coleman J, Medeiros A, D'Andrea M, Santucci T, McCormack MK. 1986. A new interstitial deletion of the long arm of chromosome 3. Am J Hum Genet 39: A124. Web of Science®Google Scholar Ogilvie MC, Rooney SC, Hodgson SV, Berry AC. 1998. Deletion of chromosome 3q proximal region gives rise to a variable phenotype. Clin Genet 53: 220–222. 10.1111/j.1399-0004.1998.tb02681.x PubMedWeb of Science®Google Scholar Okada N, Hasegawa T, Osawa M, Fukuyama Y. 1987. A case of de novo interstitial deletion 3q. J Med Genet 24: 305–308. 10.1136/jmg.24.5.305 CASPubMedWeb of Science®Google Scholar Redman JF, Seibert JJ, Page BC. 1981. Cloacal exstrophy in identical twins. Urology 17: 73–74. 10.1016/0090-4295(81)90017-0 CASPubMedWeb of Science®Google Scholar Smith NM, Chambers HM, Furness ME, Haan EA. 1992. The Oeis complex (omphalocele-exstrophy-imperforate anus-spinal defects): Recurrence in sibs. J Med Genet 29: 730–732. 10.1136/jmg.29.10.730 CASPubMedWeb of Science®Google Scholar Thauvin-Robinet C, Faivre L, Cusin V, Khau Van Kien P, Callier P, Parker KL, Fellous M, Borgnon J, Gounot E, Huet F, Sapin E, Mugneret F. 2004. Cloacal exstrophy in an infant with 9q34.1-qter deletion resulting from a de novo unbalanced translocation between chromosome 9q and Yq. Am J Med Genet 126A: 303–307. 10.1002/ajmg.a.20596 CASPubMedWeb of Science®Google Scholar Citing Literature Volume135A, Issue21 June 2005Pages 224-226 ReferencesRelatedInformation
Publication Year: 2005
Publication Date: 2005-05-10
Language: en
Type: review
Indexed In: ['crossref', 'pubmed']
Access and Citation
Cited By Count: 47
AI Researcher Chatbot
Get quick answers to your questions about the article from our AI researcher chatbot