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• W2034379074 abstract "American Journal of Medical Genetics Part AVolume 161, Issue 6 p. 1501-1504 Research Letter A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype Malgorzata Kowalczyk, Corresponding Author Malgorzata Kowalczyk Department of Medical Genetics, Medical University of Silesia, Sosnowiec, Poland Correspondence to: Malgorzata Kowalczyk, Medical University of Silesia Department of Medical Genetics Ostrogorska 30, 41-200 Sosnowiec, Poland. E-mail: [email protected]Search for more papers by this authorAgnieszka Tomaszewska, Agnieszka Tomaszewska Prenatal Diagnostic and Genetic Clinic, Zabrze, PolandSearch for more papers by this authorAgnieszka Podbiol-Palenta, Agnieszka Podbiol-Palenta Prenatal Diagnostic and Genetic Clinic, Zabrze, PolandSearch for more papers by this authorBarbara Remiszewska, Barbara Remiszewska Prenatal Diagnostic and Genetic Clinic, Zabrze, PolandSearch for more papers by this authorRobert Jan H. Galjaard, Robert Jan H. Galjaard Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The NetherlandsSearch for more papers by this authorStanislaw Zajaczek, Stanislaw Zajaczek Cytogenetic Unit, Department of Pathology, Pomeranian Medical University, Szczecin, PolandSearch for more papers by this authorMalgorzata I. Srebniak, Malgorzata I. Srebniak Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The NetherlandsSearch for more papers by this author Malgorzata Kowalczyk, Corresponding Author Malgorzata Kowalczyk Department of Medical Genetics, Medical University of Silesia, Sosnowiec, Poland Correspondence to: Malgorzata Kowalczyk, Medical University of Silesia Department of Medical Genetics Ostrogorska 30, 41-200 Sosnowiec, Poland. E-mail: [email protected]Search for more papers by this authorAgnieszka Tomaszewska, Agnieszka Tomaszewska Prenatal Diagnostic and Genetic Clinic, Zabrze, PolandSearch for more papers by this authorAgnieszka Podbiol-Palenta, Agnieszka Podbiol-Palenta Prenatal Diagnostic and Genetic Clinic, Zabrze, PolandSearch for more papers by this authorBarbara Remiszewska, Barbara Remiszewska Prenatal Diagnostic and Genetic Clinic, Zabrze, PolandSearch for more papers by this authorRobert Jan H. Galjaard, Robert Jan H. Galjaard Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The NetherlandsSearch for more papers by this authorStanislaw Zajaczek, Stanislaw Zajaczek Cytogenetic Unit, Department of Pathology, Pomeranian Medical University, Szczecin, PolandSearch for more papers by this authorMalgorzata I. Srebniak, Malgorzata I. Srebniak Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The NetherlandsSearch for more papers by this author First published: 30 April 2013 https://doi.org/10.1002/ajmg.a.35912Citations: 1Read 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 onFacebookTwitterLinkedInRedditWechat Citing Literature Volume161, Issue6June 2013Pages 1501-1504 RelatedInformation" @default.
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• W2034379074 title "A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype" @default.
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