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BioMed Research International
Volume 2015, Article ID 401941, 12 pages
http://dx.doi.org/10.1155/2015/401941
Research Article

Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects

1Postgraduate Program in Genetics and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), 91501-970 Porto Alegre, RS, Brazil
2Institute of Cardiology, University Foundation of Cardiology, Avenida Princesa Isabel 297, 90620-000 Porto Alegre, RS, Brazil
3Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Rua Ramiro Barcelos 2350, 90035-903 Porto Alegre, RS, Brazil

Received 1 March 2015; Revised 1 May 2015; Accepted 3 May 2015

Academic Editor: Jing Zhang

Copyright © 2015 Karen Regina de Souza et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [7 citations]

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  • Roberto Giugliani, Filippo P. Vairo, Mariluce Riegel, Carolina F. M. de Souza, Ida V. D. Schwartz, and Sérgio D. J. Pena, “Rare disease landscape in Brazil: report of a successful experience in inborn errors of metabolism,” Orphanet Journal of Rare Diseases, vol. 11, no. 1, 2016. View at Publisher · View at Google Scholar
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