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Interstitial deletion of the long arm of chromosome 6(q22.2q23) in a boy with phenotypic features of Williams syndrome

1989; Wiley; Volume: 35; Issue: 3 Linguagem: Inglês

10.1111/j.1399-0004.1989.tb02932.x

1399-0004

Vladimı́r Bzdúch, M Lukácová,

Williams Syndrome Research

Clinical GeneticsVolume 35, Issue 3 p. 230-231 Interstitial deletion of the long arm of chromosome 6(q22.2q23) in a boy with phenotypic features of Williams syndrome Vladimir Bzdúch, Corresponding Author Vladimir Bzdúch First Dept. Pediat., Univ. Children's Hosp. Úprkova 3 811 04 Bratislava Czechoslovakia Department of Clin. Genet. Faculty Hospital Americké nám. 3 Bratislava CzechoslovakiaSearch for more papers by this authorMargita Lukáčová, Corresponding Author Margita Lukáčová First Dept. Pediat., Univ. Children's Hosp. Úprkova 3 811 04 Bratislava Czechoslovakia Department of Clin. Genet. Faculty Hospital Americké nám. 3 Bratislava CzechoslovakiaSearch for more papers by this author Vladimir Bzdúch, Corresponding Author Vladimir Bzdúch First Dept. Pediat., Univ. Children's Hosp. Úprkova 3 811 04 Bratislava Czechoslovakia Department of Clin. Genet. Faculty Hospital Americké nám. 3 Bratislava CzechoslovakiaSearch for more papers by this authorMargita Lukáčová, Corresponding Author Margita Lukáčová First Dept. Pediat., Univ. Children's Hosp. Úprkova 3 811 04 Bratislava Czechoslovakia Department of Clin. Genet. Faculty Hospital Americké nám. 3 Bratislava CzechoslovakiaSearch for more papers by this author First published: March 1989 https://doi.org/10.1111/j.1399-0004.1989.tb02932.xCitations: 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 No abstract is available for this article. References Antia, A. U., H. E. Wiltse, R. D. Rowe, E. L. Pitt, S. Levin, O. E. Ottesen & R. E. Cooke (1967) Pathogenesis of the supravalvular aortic stenosis syndrome. J. Pediatr. 71, 431–441. 10.1016/S0022-3476(67)80308-1 CASPubMedWeb of Science®Google Scholar Burn, J. (1986) Williams syndrome. J. Med. Genet. 23, 389–395. 10.1136/jmg.23.5.389 CASPubMedWeb of Science®Google Scholar Park, J. P., J. M. Graham, S. Z. Berg & D. H. Wurster-Hill (1988) A de novo interstitial deletion of chromosome 6 (q22.2q23.1). Clin. Genet. 33, 65–68. 10.1111/j.1399-0004.1988.tb03411.x CASPubMedWeb of Science®Google Scholar Citing Literature Volume35, Issue3March 1989Pages 230-231 ReferencesRelatedInformation