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Results 1 - 20 of 45  for All Library Resources

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1
Prevalence of genetic variants associated with cardiovascular disease risk and drug response in the Southern Indian population of Kerala
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Prevalence of genetic variants associated with cardiovascular disease risk and drug response in the Southern Indian population of Kerala

Indian journal of human genetics, 2014-04, Vol.20 (2), p.175-184 [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 Apr-Jun 2014 ;Copyright: © Indian Journal of Human Genetics 2014 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.142896 ;PMID: 25400347

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2
Heritability estimation of conventional cardiovascular disease risk factors in Asian Indian families: The Calcutta family study
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Heritability estimation of conventional cardiovascular disease risk factors in Asian Indian families: The Calcutta family study

Indian journal of human genetics, 2010-01, Vol.16 (1), p.28-32 [Peer Reviewed Journal]

Copyright 2010 Indian Journal of Human Genetics. ;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: 10.4103/0971-6866.64944 ;PMID: 20838489

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3
APOA1 gene polymorphisms in the South Asian immigrant population in the United States
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APOA1 gene polymorphisms in the South Asian immigrant population in the United States

Indian journal of human genetics, 2011-09, Vol.17 (3), p.194-200 [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: 10.4103/0971-6866.92103 ;PMID: 22345992

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4
Distribution and genotype frequency of the C1431T and pro12ala polymorphisms of the peroxisome proliferator activator receptor gamma gene in an Iranian population
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Distribution and genotype frequency of the C1431T and pro12ala polymorphisms of the peroxisome proliferator activator receptor gamma gene in an Iranian population

Indian journal of human genetics, 2013-10, Vol.19 (4), p.423-429 [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: 10.4103/0971-6866.124370 ;PMID: 24497707

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5
Promoter variants in interleukin-6 and tumor necrosis factor alpha and risk of coronary artery disease in a population from Western India
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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 India

Indian 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: 24497708

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6
Association of apolipoprotein B XbaI gene polymorphism and lipid profile in northern Indian obese
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Association of apolipoprotein B XbaI gene polymorphism and lipid profile in northern Indian obese

Indian journal of human genetics, 2013-01, Vol.19 (1), p.26-31 [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: 10.4103/0971-6866.112880 ;PMID: 23901190

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7
The determination of Q192R polymorphism of paraoxonase 1 by using non-toxic substrate p-nitrophenylacetate
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The determination of Q192R polymorphism of paraoxonase 1 by using non-toxic substrate p-nitrophenylacetate

Indian 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: 23901196

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8
Paraoxonase1, its Q192R polymorphism and HDL-cholesterol in relation to intensive cardiac care unit stay in ischemic heart disease
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Paraoxonase1, its Q192R polymorphism and HDL-cholesterol in relation to intensive cardiac care unit stay in ischemic heart disease

Indian 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: 24959014

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9
Gly460Trp polymorphism of the ADD1 gene and essential hypertension in an Indian population: A meta-analysis on hypertension risk
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Gly460Trp polymorphism of the ADD1 gene and essential hypertension in an Indian population: A meta-analysis on hypertension risk

Indian journal of human genetics, 2010-01, Vol.16 (1), p.8-15 [Peer Reviewed Journal]

Copyright 2010 Indian Journal of Human Genetics. ;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: 10.4103/0971-6866.64938 ;PMID: 20838486

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10
Prevalence of congenital heart diseases in Mysore
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Prevalence of congenital heart diseases in Mysore

Indian 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: 10.4103/0971-6866.25296

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11
MCT oil-based diet reverses hypertrophic cardiomyopathy in a patient with very long chain acyl-coA dehydrogenase deficiency
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MCT oil-based diet reverses hypertrophic cardiomyopathy in a patient with very long chain acyl-coA dehydrogenase deficiency

Indian 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: 21814341

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12
A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation
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A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation

Indian 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: 23716947

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13
A rare case of congenital heart disease with ambiguous genitalia
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A rare case of congenital heart disease with ambiguous genitalia

Indian 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: 21206707

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14
Apolipoprotein E gene polymorphism and dyslipidaemia in adult Asian Indians: A population based study from Calcutta, India
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Apolipoprotein E gene polymorphism and dyslipidaemia in adult Asian Indians: A population based study from Calcutta, India

Indian journal of human genetics, 2008-09, Vol.14 (3), p.87-91 [Peer Reviewed Journal]

COPYRIGHT 2008 Medknow Publications and Media Pvt. Ltd. ;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: 10.4103/0971-6866.45000 ;PMID: 20300302

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15
Can novel Apo A-I polymorphisms be responsible for low HDL in South Asian immigrants?
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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: 20300285

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16
Genetics in public health: Rarely explored
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Genetics in public health: Rarely explored

Indian journal of human genetics, 2010-05, Vol.16 (2), p.47-54 [Peer Reviewed Journal]

Copyright 2010 Indian Journal of Human Genetics. ;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: 10.4103/0971-6866.69326 ;PMID: 21031051

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17
Epidemiology and genetics of hypertrophic cardiomyopathy
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Article
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Epidemiology and genetics of hypertrophic cardiomyopathy

Indian journal of human genetics, 2006-01, Vol.12 (1), p.26-33 [Peer Reviewed Journal]

Copyright 2006 Indian Journal of Human Genetics. ;Copyright Medknow Publications 2006 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.25299

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18
Genetic variation in exon 5 of troponin - I gene in hypertrophic cardiomyopathy cases
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Genetic variation in exon 5 of troponin - I gene in hypertrophic cardiomyopathy cases

Indian journal of human genetics, 2007-05, Vol.13 (2), p.50-53 [Peer Reviewed Journal]

Copyright 2007 Indian Journal of Human Genetics. ;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: 10.4103/0971-6866.34706 ;PMID: 21957345

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19
Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
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Missense mutation G296S in GATA4 is not responsible for cardiac septal defects

Indian 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: 21957339

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20
MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India
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MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India

Indian journal of human genetics, 2009-05, Vol.15 (2), p.60-64 [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: 10.4103/0971-6866.55217 ;PMID: 20680153

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