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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Analysis of next generation sequencing data in two complementary UK populations with congenital heart diseaseDigital Resources/Online E-Resources |
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Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease (vol 17, e1009679, 2021)PLOS GENETICS, 2021, Vol.17 (9)ISSN: 1553-7404 ;EISSN: 1553-7404Full text available |
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Population and Molecular Genetic Studies of Congenital Heart DiseaseDigital Resources/Online E-Resources |
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Replacement therapy for iron deficiency improves exercise capacity and quality of life in patients with cyanotic congenital heart disease and/or the Eisenmenger syndromeopen access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades. https://creativecommons.org/licenses/by-nc-nd/3.0Digital Resources/Online E-Resources |
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CCA development in the background of Congenital Hepatic Fibrosis/Caroli DiseaseThe Author(s)Digital Resources/Online E-Resources |
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Radiologic Diagnosis of Congenital Heart Disease in ChildrenVCU. Licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. http://creativecommons.org/licenses/by-nc-sa/3.0 Acknowledgement of the Virginia Commonwealth University Libraries as a source is required.Digital Resources/Online E-Resources |
| 7 |
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Progress of Congenital Heart Disease: The Team Approach as It Includes the AnesthesiologistVCU. Licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. http://creativecommons.org/licenses/by-nc-sa/3.0 Acknowledgement of the Virginia Commonwealth University Libraries as a source is required.Digital Resources/Online E-Resources |
| 8 |
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Sebelipasa alfa per al tractament del dèficit de lipasa àcida lisosòmicaAttribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccessDigital Resources/Online E-Resources |
| 9 |
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Programa de detecció precoç neonatal: Catalunya, 1982-2010Atribución-NoComercial-SinDerivadas 3.0 España http://creativecommons.org/licenses/by-nc-nd/3.0/es/ info:eu-repo/semantics/openAccessDigital Resources/Online E-Resources |
| 10 |
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Ordenació del consell genètic i de les anàlisis genètiques en trastorns o malalties genètiques constitutives i somàtiques: unitats d'alta especialització (06/2015)Atribución-NoComercial-SinDerivadas 3.0 España http://creativecommons.org/licenses/by-nc-nd/3.0/es/ info:eu-repo/semantics/openAccessDigital Resources/Online E-Resources |
| 11 |
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Recent Techniques in Echocardiography: Two-Dimensional EchocardiographyVCU. Licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. http://creativecommons.org/licenses/by-nc-sa/3.0 Acknowledgement of the Virginia Commonwealth University Libraries as a source is required.Digital Resources/Online E-Resources |
| 12 |
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Determinants of penetrance and variable expressivity in genetic ophthalmic disordersDigital Resources/Online E-Resources |
| 13 |
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Programa de diagnòstic prenatal d'anomalies congènites fetals a Catalunya (07/2008)Atribución-NoComercial-SinDerivadas 3.0 España http://creativecommons.org/licenses/by-nc-nd/3.0/es/ info:eu-repo/semantics/openAccessDigital Resources/Online E-Resources |
| 14 |
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Social functioning and behaviour in mucopolysaccharidosis type I and other developmental genetic disordersDigital Resources/Online E-Resources |
| 15 |
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Passive immunization during pregnancy for congenital cytomegalovirus infectionFrom The New England Journal of Medicine, Nigro, G., Adler, S.P., La Torre, R., et al., Passive immunization during pregnancy for congenital cytomegalovirus infection, Vol. 353, Page 1350, Copyright © 2005 Massachusetts Medical Society. Reprinted with permission.Digital Resources/Online E-Resources |
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| 17 |
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Twenty Years Ago Scientists Stunned The World When They Could Decode The Genes That Make Up A Human Being, CBS60 Minutes, 2020Content and programming Copyright MMXX CBS Broadcasting Inc. ALL RIGHTS RESERVED. Copyright 2020 ASC Services II Media, LLC. All materials herein are protected by United States copyright law and may not be reproduced, distributed, transmitted, displayed, published or broadcast without the prior written permission of ASC Services II Media, LLC. You may not alter or remove any trademark, copyright or other notice from copies of the content. ;ISSN: 0361-3216Full text available |
| 18 |
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Twenty Years Ago Scientists Stunned The World With When The Announced They Had Decoded The Genes That Make Up A Human Being, CBS60 Minutes, 2020Content and programming Copyright MMXX CBS Broadcasting Inc. ALL RIGHTS RESERVED. Copyright 2020 ASC Services II Media, LLC. All materials herein are protected by United States copyright law and may not be reproduced, distributed, transmitted, displayed, published or broadcast without the prior written permission of ASC Services II Media, LLC. You may not alter or remove any trademark, copyright or other notice from copies of the content. ;ISSN: 0361-3216Full text available |
| 19 |
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Special Issue "Genetic Advances in Neuromuscular Disorders : From Gene Identification to Gene Therapy"open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by/4.0Digital Resources/Online E-Resources |
| 20 |
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Arabian Medical Genetics: Of Rare Disorders and Decreasing Oil RentDistributed under a Creative Commons Attribution 4.0 International LicenseDigital Resources/Online E-Resources |
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