Abstract
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: 22AboutPDF 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 onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume35, Issue3March 1989Pages 230-231 RelatedInformation
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