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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Article
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Prevalence of congenital heart diseases in MysoreIndian journal of human genetics, 2006-01, Vol.12 (1), p.11-16 [Peer Reviewed Journal]Copyright 2006 Indian Journal of Human Genetics. ;Copyright Medknow Publications 2006 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.25296Full text available |
| 2 |
Material Type: Article
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MCT oil-based diet reverses hypertrophic cardiomyopathy in a patient with very long chain acyl-coA dehydrogenase deficiencyIndian journal of human genetics, 2011-01, Vol.17 (1), p.29-32 [Peer Reviewed Journal]COPYRIGHT 2011 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2011 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd 2011 ;Indian Journal of Human Genetics 2011 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.82190 ;PMID: 21814341Full text available |
| 3 |
Material Type: Article
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Novel mutations in arrhythmogenic right ventricular cardiomyopathy from Indian populationIndian journal of human genetics, 2011-05, Vol.17 (2), p.70-76 [Peer Reviewed Journal]COPYRIGHT 2011 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2011 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd 2011 ;Copyright: © Indian Journal of Human Genetics 2011 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.86182 ;PMID: 22090716Full text available |
| 4 |
Material Type: Article
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Linkage analysis of three families with arrythmogenic right ventricular cardiomyopathy in IndiaIndian journal of human genetics, 2009-05, Vol.15 (2), p.54-59 [Peer Reviewed Journal]COPYRIGHT 2009 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2009 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt. Ltd. 2009 ;Indian Journal of Human Genetics 2010 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.55216 ;PMID: 20680152Full text available |
| 5 |
Material Type: Article
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A rare case of congenital heart disease with ambiguous genitaliaIndian journal of human genetics, 2011-04, Vol.16 (3) [Peer Reviewed Journal]Copyright 2010 Indian Journal of Human Genetics. ;ISSN: 0971-6866 ;EISSN: 1998-362XFull text available |
| 6 |
Material Type: Article
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Dysmorphic features and congenital heart disease in chromosome 6q deletion: A short reportIndian journal of human genetics, 2012-01, Vol.18 (1), p.127-129 [Peer Reviewed Journal]Copyright 2012 Indian Journal of Human Genetics. ;COPYRIGHT 2012 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2012 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd 2012 ;Copyright: © Indian Journal of Human Genetics 2012 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.96682 ;PMID: 22754239Full text available |
| 7 |
Material Type: Article
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Promoter variants in interleukin-6 and tumor necrosis factor alpha and risk of coronary artery disease in a population from Western IndiaIndian journal of human genetics, 2013-10, Vol.19 (4), p.430-436 [Peer Reviewed Journal]COPYRIGHT 2013 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2013 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd Oct-Dec 2013 ;Copyright: © Indian Journal of Human Genetics 2013 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.124371 ;PMID: 24497708Full text available |
| 8 |
Material Type: Article
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A rare case of congenital heart disease with ambiguous genitaliaIndian journal of human genetics, 2010-09, Vol.16 (3), p.166-168 [Peer Reviewed Journal]COPYRIGHT 2010 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2010 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt. Ltd. 2010 ;Indian Journal of Human Genetics 2010 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.73414 ;PMID: 21206707Full text available |
| 9 |
Material Type: Article
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The determination of Q192R polymorphism of paraoxonase 1 by using non-toxic substrate p-nitrophenylacetateIndian journal of human genetics, 2013-01, Vol.19 (1), p.71-77 [Peer Reviewed Journal]COPYRIGHT 2013 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2013 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd Jan-Mar 2013 ;Copyright: © Indian Journal of Human Genetics 2013 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.112897 ;PMID: 23901196Full text available |
| 10 |
Material Type: Article
|
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Paraoxonase1, its Q192R polymorphism and HDL-cholesterol in relation to intensive cardiac care unit stay in ischemic heart diseaseIndian journal of human genetics, 2014-01, Vol.20 (1), p.51-58 [Peer Reviewed Journal]COPYRIGHT 2014 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2014 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd Jan-Mar 2014 ;Copyright: © Indian Journal of Human Genetics 2014 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.132756 ;PMID: 24959014Full text available |
| 11 |
Material Type: Article
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A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardationIndian journal of human genetics, 2012-09, Vol.18 (3), p.352-355 [Peer Reviewed Journal]COPYRIGHT 2012 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2012 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd 2012 ;Copyright: © Indian Journal of Human Genetics 2012 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.108033 ;PMID: 23716947Full text available |
| 12 |
Material Type: Article
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Can novel Apo A-I polymorphisms be responsible for low HDL in South Asian immigrants?Indian journal of human genetics, 2008-01, Vol.14 (1), p.9-15 [Peer Reviewed Journal]Copyright 2008 Indian Journal of Human Genetics. ;COPYRIGHT 2008 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications 2008 ;Indian Journal of Human Genetics 2008 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.42321 ;PMID: 20300285Full text available |
| 13 |
Material Type: Article
|
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Missense mutation G296S in GATA4 is not responsible for cardiac septal defectsIndian journal of human genetics, 2007-01, Vol.13 (1), p.30-32 [Peer Reviewed Journal]COPYRIGHT 2007 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2007 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications 2007 ;Indian Journal of Human Genetics 2007 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.32032 ;PMID: 21957339Full text available |
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