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- W2007136061 abstract "American Journal of Medical GeneticsVolume 57, Issue 3 p. 501-503 Letter to the Editor Hungarian case with Costello syndrome and translocation t(1,22) Andrew E. Czeizel, Corresponding Author Andrew E. Czeizel Department of Human Genetics National Institute of Hygiene–WHO Collaborating Centre for the Community Control of Hereditary Disease Budapest, HungaryH-1966, OKI Gyáli út 2–6., Budapest, HungarySearch for more papers by this authorLászló Tímár, László Tímár Department of Human Genetics National Institute of Hygiene–WHO Collaborating Centre for the Community Control of Hereditary Disease Budapest, HungarySearch for more papers by this author Andrew E. Czeizel, Corresponding Author Andrew E. Czeizel Department of Human Genetics National Institute of Hygiene–WHO Collaborating Centre for the Community Control of Hereditary Disease Budapest, HungaryH-1966, OKI Gyáli út 2–6., Budapest, HungarySearch for more papers by this authorLászló Tímár, László Tímár Department of Human Genetics National Institute of Hygiene–WHO Collaborating Centre for the Community Control of Hereditary Disease Budapest, HungarySearch for more papers by this author First published: 3 July 1995 https://doi.org/10.1002/ajmg.1320570331Citations: 24AboutPDF 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 Borochowitz Z, Pavone L, Mazor G, Rizzo R, Dar H (1992): New multiple congenital anomalies: mental retardation syndrome (MCA/ MR) with facio-cutaneous-skeletal involvement. Am J Med Genet 43: 678–685. Costello JM (1977): A new syndrome: mental subnormality and nasal papillomata. Aust Paediat 13: 114–118. Koppe R, Kaplan P, Hunter A, MacMurray B (1989): Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF) syndrome. Am J Med Genet 34: 305–312. Lurie JW (1994): Genetics of the Costello syndrome. Am J Med Genet 52: 358–359. Philip N, Mancini JC (1993): Costello syndrome and facio-cutaneous-skeletal syndrome. Am J Med Genet 47: 174–175. Teebi AS (1993): Costello or facio-cutaneous-skeletal syndrome. Am J Med Genet 47: 172. Zampino G, Mastroiacovo P, Ricci R, Zolli M, Segni G, Martini-Neri ME, Neri G (1993): Costello syndrome: Further clinical delineation, natural history, genetic definition, and nosology. Am J Med Genet 47: 176–183. Citing Literature Volume57, Issue33 July 1995Pages 501-503 ReferencesRelatedInformation" @default.
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- W2007136061 title "Hungarian case with Costello syndrome and translocation t(1,22)" @default.
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