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  Citation statistics : Table of Contents
   2013| October-December  | Volume 19 | Issue 4  
    Online since January 4, 2014

 
 
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CASE REPORTS
Double heterozygous hemoglobin Q India/hemoglobin D Punjab hemoglobinopathy: Report of two rare cases
Deepti Mutreja, Seema Tyagi, Narender Tejwani, Jasmita Dass
October-December 2013, 19(4):479-482
DOI:10.4103/0971-6866.124381  PMID:24497718
  1 2,201 65
A case report of ectopia cordis and omphalocele
Amar M Taksande, Krishna Y Vilhekar
October-December 2013, 19(4):491-493
DOI:10.4103/0971-6866.124384  PMID:24497721
  1 1,214 47
ORIGINAL ARTICLES
Mutation analysis of mitogen activated protein kinase 1 gene in Indian cases of 46,XY disorder of sex development
Dhanjit Kumar Das, Subodh G Rahate, Bhakti P Mehta, Harshavardhan M Gawde, Parag M Tamhankar
October-December 2013, 19(4):437-442
DOI:10.4103/0971-6866.124372  PMID:24497709
  1 1,381 47
Genetic variants in the cytochrome P450 2D6 gene in the Sri Lankan population
T. D. Praveen Tharanga, C. M. V. Jinadasa, MF Risama, Priyadarshani Galappatthy, RL Jayakody, Vajira H. W. Dissanayake
October-December 2013, 19(4):392-396
DOI:10.4103/0971-6866.124361  PMID:24497701
  1 2,015 84
Protein tyrosine phosphatase non-receptor type 22 gene polymorphism C1858T is not associated with leprosy in Azerbaijan, Northwest Iran
Mohammad Reza Aliparasti, Shohreh Almasi, Jafar Majidi, Fatemeh Zamani, Ali Reza Khoramifar, Ali Reza Farshi Azari
October-December 2013, 19(4):403-407
DOI:10.4103/0971-6866.124365  PMID:24497703
  1 895 38
CASE REPORTS
An incidental case of dihydropyrimidine dehydrogenase deficiency: One case, multiple challenges
Hamoud H Al Khallaf, Miao He, Angela Wittenauer, Elizabeth E Woolley, Mariagrazia Cunto, Muhammad Ali Pervaiz
October-December 2013, 19(4):483-486
DOI:10.4103/0971-6866.124382  PMID:24497719
  - 1,406 21
Dyschromatosis universalis hereditaria: Infrequent genodermatoses in India
Hari Kishan Kumar Yadalla, Srivalli Pinninti, Anagha Ramesh Babu
October-December 2013, 19(4):487-490
DOI:10.4103/0971-6866.124383  PMID:24497720
  - 1,170 41
A rare anomaly of the foot presented as polydactyly
Vikram Jeet Singh Dhingra, Ashish Kumar, Amit Mittal, Samita Gupta, Rikki Singal, Bir Singh, Chetan Dua
October-December 2013, 19(4):469-471
DOI:10.4103/0971-6866.124378  PMID:24497715
  - 1,665 48
Aromatase excess syndrome presenting with prepubertal gynecomastia in an Egyptian child with type 1 neurofibromatosis
Kotb Abbass Metwalley, Hekma Saad Farghaly
October-December 2013, 19(4):472-474
DOI:10.4103/0971-6866.124379  PMID:24497716
  - 3,926 38
Molecular characterization in a case of isolated growth hormone deficiency and further prenatal diagnosis of an unborn sibling
Ruchi Nadar, Kavita Khatod, Nikhil Phadke, Chaitanya Datar, Sujata Vaidya, Anuradha Khadilkar, Vaman Khadilkar
October-December 2013, 19(4):475-478
DOI:10.4103/0971-6866.124380  PMID:24497717
  - 1,221 48
EDITORIAL
Innumerable studies on single nucleotide polymorphisms: What could be its utility?
K Ghosh, Ajit Gorakshakar
October-December 2013, 19(4):381-383
DOI:10.4103/0971-6866.124354  PMID:24497699
  - 2,133 99
LETTERS TO THE EDITOR
Influenza A H1N1 hemagglutinin and human axon guidance proteins: Peptide sharing but not same epitopes
Somsri Wiwanitkit, Viroj Wiwanitkit
October-December 2013, 19(4):512-512
DOI:10.4103/0971-6866.124386  PMID:24497723
  - 510 17
Deoxyribonucleic acid profiling in forensic dental identification
Thorakkal Shamim
October-December 2013, 19(4):513-513
DOI:10.4103/0971-6866.124387  PMID:24497724
  - 2,865 38
META ANALYSIS
Deoxyribonucleic acid repair gene X-ray repair cross-complementing group 1 polymorphisms and non-carcinogenic disease risk in different populations: A meta-analysis
Bagher Larijani, Javad Mohammadi Asl, Abbas Keshtkar, Najmaldin Saki, Fatemeh Ardeshir Larijani, Fakher Rahim
October-December 2013, 19(4):494-511
PMID:24497722
  - 1,152 21
ORIGINAL ARTICLES
Deoxyribonucleic acid damage study in primary amenorrhea by comet assay and karyotyping
Sarah Ramamurthy, Parkash Chand, Latha Chaturvedula, K Ramachandra Rao
October-December 2013, 19(4):397-402
DOI:10.4103/0971-6866.124363  PMID:24497702
  - 912 54
Genetic polymorphisms of estrogen receptor alpha and catechol-O-methyltransferase genes in Turkish patients with familial prostate carcinoma
Ayfer Pazarbasi, M Bertan Yilmaz, Davut Alptekin, Umit Luleyap, Zuhtu Tansug, Lutfiye Ozpak, Muzeyyen Izmirli, Dilge Onatoglu-Arikan, Sabriye Kocaturk-Sel, Mehmet Ali Erkoc, Ozgur Turgut, Ceyhun Bereketoglu, Erdal Tunc, Eylul Akbal
October-December 2013, 19(4):408-411
DOI:10.4103/0971-6866.124366  PMID:24497704
  - 865 33
Prevalence of methylenetetrahydrofolate reductase 677 C-T polymorphism among mothers of Down syndrome children
Anupam Kaur, Amandeep Kaur
October-December 2013, 19(4):412-414
DOI:10.4103/0971-6866.124368  PMID:24497705
  - 1,014 60
Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study
Frenny J Sheth, Thomas Liehr, Pritti Kumari, Ralph Akinde, Harsh J Sheth, Jayesh J Sheth
October-December 2013, 19(4):415-422
DOI:10.4103/0971-6866.124369  PMID:24497706
  - 2,232 108
Distribution and genotype frequency of the C1431T and pro12ala polymorphisms of the peroxisome proliferator activator receptor gamma gene in an Iranian population
Hassan Rooki, Monir-Sadat Haerian, Pedram Azimzadeh, Mahmoud Ebrahimi, Reza Mirhafez, Gordon Ferns, Majid Ghayour-Mobarhan, Mohammad-Reza Zali
October-December 2013, 19(4):423-429
DOI:10.4103/0971-6866.124370  PMID:24497707
  - 1,061 36
Promoter variants in interleukin-6 and tumor necrosis factor alpha and risk of coronary artery disease in a population from Western India
Aparna A Bhanushali, BR Das
October-December 2013, 19(4):430-436
DOI:10.4103/0971-6866.124371  PMID:24497708
  - 963 36
Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization
Farkhondeh Behjati, Saghar Ghasemi Firouzabadi, Roxana Kariminejad, Roshanak Vameghi, Firouzeh Sajedi, Yousef Shafaghati, Behruz Ebrahimizade Ghasemlou, Azadeh Shojaei, Peyman Jamali, Ideh Bahman, Hossein Najmabadi
October-December 2013, 19(4):443-448
DOI:10.4103/0971-6866.124373  PMID:24497710
  - 1,197 38
Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population
Rajeev Kumar Pandey, Minu Bajpai, Abid Ali, Sukanya Gayan, Amit Singh
October-December 2013, 19(4):449-453
DOI:10.4103/0971-6866.124374  PMID:24497711
  - 1,105 51
The proportion of tetrahydrobiopterin deficiency and PAH gene deficiency variants among cases with hyperphenyalaninemia in Western Iran
Keyvan Moradi, Reza Alibakhshi, Shohreh Khatami
October-December 2013, 19(4):454-458
DOI:10.4103/0971-6866.124375  PMID:24497712
  - 1,175 22
Msx1 Gene Variant - its Association in Isolated Hypodontia: A Case Control Genetic study!!!
Naveen Admala Reddy, Gopinath Adusumilli, Raghu Devanna, Rohra G Mayur, Saravanan Pichai, Sharmila Arujnan
October-December 2013, 19(4):459-464
DOI:10.4103/0971-6866.124376  PMID:24497713
  - 987 51
Analysis of association of TaqI VDR gene polymorphism with the chronic periodontitis in Dravidian ethnicity
Gurumoorthy Kaarthikeyan, ND Jayakumar, O Padmalatha, Sheeja Varghese, B Anand
October-December 2013, 19(4):465-468
DOI:10.4103/0971-6866.124377  PMID:24497714
  - 766 39
REVIEW ARTICLES
Epigenetics in the nervous system: An overview of its essential role
Bhavya Ravi, Manoj Kannan
October-December 2013, 19(4):384-391
DOI:10.4103/0971-6866.124357  PMID:24497700
  - 2,492 97
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