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Material Type: Article
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Serial Magnetic Resonance Imaging for Aortic Dilation in Tetralogy of Fallot With Pulmonary StenosisThe American journal of cardiology, 2023-03, Vol.191, p.92-100 [Peer Reviewed Journal]2022 Elsevier Inc. ;Copyright © 2022 Elsevier Inc. All rights reserved. ;2022. Elsevier Inc. ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2022.12.015 ;PMID: 36669383Full text available |
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Material Type: Article
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Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathwaysPLoS genetics, 2012-08, Vol.8 (8), p.e1002843-e1002843 [Peer Reviewed Journal]COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;Silversides et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Silversides CK, Lionel AC, Costain G, Merico D, Migita O, et al. (2012) Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways. PLoS Genetics 8(8): e1002843. doi:10.1371/journal.pgen.1002843 ;2012 Silversides et al 2012 Silversides et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002843 ;PMID: 22912587Full text available |
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Material Type: Article
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Comprehensive genotype–phenotype analysis in 230 patients with tetralogy of FallotJournal of medical genetics, 2010-05, Vol.47 (5), p.321-331 [Peer Reviewed Journal]2010, Published by the BMJ Publishing Group Limited For permission to use, (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;2015 INIST-CNRS ;Copyright: 2010 (c) 2010, Published by the BMJ Publishing Group Limited For permission to use, (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.2009.070391 ;PMID: 19948535 ;CODEN: JMDGAEFull text available |
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Material Type: Article
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Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twinsPrenatal diagnosis, 2018-04, Vol.38 (5), p.318 [Peer Reviewed Journal]2018 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5238 ;PMID: 29460287Digital Resources/Online E-Resources |
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Material Type: Article
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Chromosomal abnormalities among children born with conotruncal cardiac defectsBirth defects research. A Clinical and molecular teratology, 2009-01, Vol.85 (1), p.30-35 [Peer Reviewed Journal]Copyright © 2008 Wiley‐Liss, Inc. ;ISSN: 1542-0752 ;EISSN: 1542-0760 ;DOI: 10.1002/bdra.20541 ;PMID: 19067405Full text available |
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Material Type: Article
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Implantation of the Melody Transcatheter Pulmonary Valve in Patients With a Dysfunctional Right Ventricular Outflow Tract Conduit: Early Results From the U.S. Clinical TrialJournal of the American College of Cardiology, 2009-10, Vol.54 (18), p.1722-1729 [Peer Reviewed Journal]2009 INIST-CNRS ;Copyright Elsevier Limited Oct 27, 2009 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2009.06.034 ;PMID: 19850214 ;CODEN: JACCDIFull text available |
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Material Type: Article
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Foetal echocardiographic assessment of tetralogy of Fallot and post-natal outcomeEuropean heart journal, 2008-06, Vol.29 (11), p.1432-1438 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2008. For permissions please email: journals.permissions@oxfordjournals.org 2008 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2008. For permissions please email: journals.permissions@oxfordjournals.org ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehn194 ;PMID: 18467321Full text available |
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Material Type: Article
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Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart DiseaseGenes, 2019-08, Vol.10 (9), p.663 [Peer Reviewed Journal]2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 by the authors. 2019 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes10090663 ;PMID: 31480262Full text available |