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1
Tuberous sclerosis with rhabdomyoma
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Article
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Tuberous sclerosis with rhabdomyoma

Indian journal of human genetics, 2013-01, Vol.19 (1), p.93-95 [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: 10.4103/0971-6866.112912 ;PMID: 23901201

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2
Cytogenetic abnormalities in 222 infertile men with azoospermia and oligospermia in Iran: Report and review
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Article
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Cytogenetic abnormalities in 222 infertile men with azoospermia and oligospermia in Iran: Report and review

Indian journal of human genetics, 2012-05, Vol.18 (2), p.198-203 [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: 10.4103/0971-6866.100764 ;PMID: 23162296

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3
Frequency of twinning in southwest Nigeria
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Article
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Frequency of twinning in southwest Nigeria

Indian journal of human genetics, 2008-05, Vol.14 (2), p.41-47 [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: 10.4103/0971-6866.44104 ;PMID: 20300293

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4
Neural tube defects between folate metabolism and genetics
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Article
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Neural tube defects between folate metabolism and genetics

Indian journal of human genetics, 2012-02, Vol.17 (3) [Peer Reviewed Journal]

Copyright 2011 Indian Journal of Human Genetics. ;ISSN: 0971-6866 ;EISSN: 1998-362X

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5
Neural tube defects between folate metabolism and genetics
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Article
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Neural tube defects between folate metabolism and genetics

Indian journal of human genetics, 2011-09, Vol.17 (3), p.126-131 [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: 10.4103/0971-6866.92082 ;PMID: 22345982

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6
Molecular investigation of mental retardation locus gene PRSS12 by linkage analysis
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Article
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Molecular investigation of mental retardation locus gene PRSS12 by linkage analysis

Indian journal of human genetics, 2011-05, Vol.17 (2), p.65-69 [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: 10.4103/0971-6866.86178 ;PMID: 22090715

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7
Protein tyrosine phosphatase non-receptor type 22 gene polymorphism C1858T is not associated with leprosy in Azerbaijan, Northwest Iran
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Article
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Protein tyrosine phosphatase non-receptor type 22 gene polymorphism C1858T is not associated with leprosy in Azerbaijan, Northwest Iran

Indian journal of human genetics, 2013-10, Vol.19 (4), p.403-407 [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: 10.4103/0971-6866.124365 ;PMID: 24497703

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8
Investigation of chromosomal aberrations in Egyptian hepatocellular carcinoma patients by fluorescence in situ hybridization
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Article
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Investigation of chromosomal aberrations in Egyptian hepatocellular carcinoma patients by fluorescence in situ hybridization

Indian journal of human genetics, 2010-05, Vol.16 (2), p.87-93 [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: 10.4103/0971-6866.69370 ;PMID: 21031057

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9
Characterization of cryptic rearrangements, deletion, complex variants of PML, RARA in acute promyelocytic leukemia
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Article
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Characterization of cryptic rearrangements, deletion, complex variants of PML, RARA in acute promyelocytic leukemia

Indian journal of human genetics, 2011-05, Vol.17 (2), p.54-58 [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: 10.4103/0971-6866.86174 ;PMID: 22090713

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10
Genetic variation in exon 5 of troponin - I gene in hypertrophic cardiomyopathy cases
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Article
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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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11
Effect of maternal Tp53 gene G412C polymorphism on neural tube defects: A study from North India
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Article
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Effect of maternal Tp53 gene G412C polymorphism on neural tube defects: A study from North India

Indian journal of human genetics, 2012-05, Vol.18 (2), p.177-182 [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: 10.4103/0971-6866.100757 ;PMID: 23162292

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12
Consanguinity and chromosomal abnormality
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Article
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Consanguinity and chromosomal abnormality

Indian journal of human genetics, 2005-05, Vol.11 (2), p.108 [Peer Reviewed Journal]

COPYRIGHT 2005 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications 2005 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.16812

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13
G-C heterozygosis in mutS homolog2 as a risk factor to hereditary nonpolyposis colon cancer in the absence of a family medical history
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Article
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G-C heterozygosis in mutS homolog2 as a risk factor to hereditary nonpolyposis colon cancer in the absence of a family medical history

Indian journal of human genetics, 2011-05, Vol.17 (2), p.90-93 [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: 10.4103/0971-6866.86191 ;PMID: 22090720

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14
Genetics in public health: Rarely explored
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Article
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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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15
Human sex ratio at birth in South West Nigeria
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Article
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Human sex ratio at birth in South West Nigeria

Indian journal of human genetics, 2007-05, Vol.13 (2), p.59-64 [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: 10.4103/0971-6866.34708 ;PMID: 21957347

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16
A case of primary amenorrhea with 46+XY genotype from Kashmir Valley
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Article
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A case of primary amenorrhea with 46+XY genotype from Kashmir Valley

Indian journal of human genetics, 2013-07, Vol.19 (3), p.360-362 [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 Jul-Sep 2013 ;Copyright: © Indian Journal of Human Genetics 2013 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.120816 ;PMID: 24339555

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17
Loss of sex chromosome in acute myeloid leukemia
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Article
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Loss of sex chromosome in acute myeloid leukemia

Indian journal of human genetics, 2004-01, Vol.10 (1), p.22 [Peer Reviewed Journal]

Copyright 2004 Indian Journal of Human Genetics. ;COPYRIGHT 2004 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications 2004 ;ISSN: 0971-6866 ;EISSN: 1998-362X

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18
Genetic heterogeneity of population structure in 15 major scheduled tribes in central-eastern India: A study of immuno-hematological disorders
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Article
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Genetic heterogeneity of population structure in 15 major scheduled tribes in central-eastern India: A study of immuno-hematological disorders

Indian journal of human genetics, 2006-05, Vol.12 (2), p.86-92 [Peer Reviewed Journal]

COPYRIGHT 2006 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2006 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications 2006 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.27792

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19
Identification of a rare blood group, "Bombay (Oh) phenotype," in Bhuyan tribe of Northwestern Orissa, India
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Article
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Identification of a rare blood group, "Bombay (Oh) phenotype," in Bhuyan tribe of Northwestern Orissa, India

Indian journal of human genetics, 2007-09, Vol.13 (3), p.109-113 [Peer Reviewed Journal]

COPYRIGHT 2007 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2007 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications 2007 ;Copyright: © Indian Journal of Human Genetics 2007 ;ISSN: 0971-6866 ;EISSN: 1998-362X ;DOI: 10.4103/0971-6866.38985 ;PMID: 21957358

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20
Association of single nucleotide polymorphisms of CACNA1A gene in migraine
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Article
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Association of single nucleotide polymorphisms of CACNA1A gene in migraine

Indian journal of human genetics, 2014-01, Vol.20 (1), p.59-63 [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: 10.4103/0971-6866.132757 ;PMID: 24959015

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