Indian Journal of Human Genetics
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   2014| January-March  | Volume 20 | Issue 1  
    Online since May 19, 2014

 
 
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REVIEW ARTICLE
Reactive metabolites and antioxidant gene polymorphisms in type 2 diabetes mellitus
Monisha Banerjee, Pushpank Vats
January-March 2014, 20(1):10-19
DOI:10.4103/0971-6866.132747  PMID:24959009
  3,037 160 3
Neurotransmitters in alcoholism: A review of neurobiological and genetic studies
Niladri Banerjee
January-March 2014, 20(1):20-31
DOI:10.4103/0971-6866.132750  PMID:24959010
  2,682 87 1
Genes and oral cancer
Sunit Kumar Jurel, Durga Shanker Gupta, Raghuwar D. Singh, Mrinalini Singh, Shilpi Srivastava
January-March 2014, 20(1):4-9
DOI:10.4103/0971-6866.132745  PMID:24959008
  1,665 172 -
CASE REPORTS
Poland syndrome
Chandra Madhur Sharma, Shrawan Kumar, Manoj K. Meghwani, Ravi P. Agrawal
January-March 2014, 20(1):82-84
DOI:10.4103/0971-6866.132764  PMID:24959021
  1,689 46 -
ORIGINAL ARTICLES
A comprehensive analysis of breakpoint cluster region-abelson fusion oncogene splice variants in chronic myeloid leukemia and their correlation with disease biology
Zafar Iqbal
January-March 2014, 20(1):64-68
DOI:10.4103/0971-6866.132758  PMID:24959016
  1,543 76 -
EDITORIAL
Familial Mediterranean fever: An unusual disease enlightening the inflammation biology
Kanjaksha Ghosh, Ajit C Gorakshakar
January-March 2014, 20(1):1-3
DOI:10.4103/0971-6866.132741  PMID:24959007
  1,445 105 -
BRIEF REPORTS
Split-hand/feet malformation in three tamilian families and review of the reports from India
S. Deepak Amalnath, Maya Gopalakrishnan, Tarun Kumar Dutta
January-March 2014, 20(1):92-95
DOI:10.4103/0971-6866.132769  PMID:24959024
  1,484 60 -
ORIGINAL ARTICLES
Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children' Hospital, Mansoura, Egypt
Mohammad S. Al-Haggar, Sohier Yahia, Dina Abdel-Hady, Afaf Al-Saied, Rasha Al-Kenawy, Rabab Abo-El-Kasem
January-March 2014, 20(1):43-50
DOI:10.4103/0971-6866.132755  PMID:24959013
  1,375 47 1
CASE REPORTS
Raine syndrome
B. Vishwanath, K. Srinivasa, M. Veera Shankar
January-March 2014, 20(1):72-74
DOI:10.4103/0971-6866.132761  PMID:24959018
  1,295 71 1
ORIGINAL ARTICLES
Association of single nucleotide polymorphisms of CACNA1A gene in migraine
Aadil Bashir, Shiekh Saleem, Maqbool Wani, Roohi Rasool, Irfan Yousuf Wani, Azhara Gulnar, Sawan Verma
January-March 2014, 20(1):59-63
DOI:10.4103/0971-6866.132757  PMID:24959015
  1,151 71 -
Association study of the ABCC8 gene variants with type 2 diabetes in south Indians
Radha Venkatesan, Dhanasekaran Bodhini, Nagarajan Narayani, Viswanathan Mohan
January-March 2014, 20(1):37-42
DOI:10.4103/0971-6866.132752  PMID:24959012
  1,079 103 -
CASE REPORTS
Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies
Abdelhafid Natiq, Siham Chafai Elalaoui, Thomas Liehr, Sad Amzazi, Abdelaziz Sefiani
January-March 2014, 20(1):89-91
DOI:10.4103/0971-6866.132767  PMID:24959023
  1,108 49 1
ORIGINAL ARTICLES
Pattern of chromosome involvement in childhood hyperdiploid pre-B-cell acute lymhoblastic leukemia cases from India
Lily S. Kerketta, Vundinti Baburao, Kanjaksha Ghosh
January-March 2014, 20(1):32-36
DOI:10.4103/0971-6866.132751  PMID:24959011
  1,071 73 -
CASE REPORTS
Chronic myeloid leukemia in case of Klinefelter syndrome
Vasundhara Chennuri, Rajesh Kashyap, Parag Tamhankar, Subha Phadke
January-March 2014, 20(1):69-71
DOI:10.4103/0971-6866.132760  PMID:24959017
  1,065 63 -
A novel chromosomal abnormality t (9;14)(p24;q13) in B-acute lymphoblastic leukemia
Sureshkumar Raveendran, Santhi Sarojam, Geetha Narayanan, Hariharan Sreedharan
January-March 2014, 20(1):79-81
DOI:10.4103/0971-6866.132763  PMID:24959020
  990 53 -
Berardinelli-Seip syndrome type 1 in an Egyptian child
Kotb Abbass Metwalley, Hekma Saad Farghaly
January-March 2014, 20(1):75-78
DOI:10.4103/0971-6866.132762  PMID:24959019
  977 46 1
ORIGINAL ARTICLES
Paraoxonase1, its Q192R polymorphism and HDL-cholesterol in relation to intensive cardiac care unit stay in ischemic heart disease
Mahesh Harishchandra Hampe, Mukund Ramchandra Mogarekar
January-March 2014, 20(1):51-58
DOI:10.4103/0971-6866.132756  PMID:24959014
  908 64 -
CASE REPORTS
Unexpected Inheritance of a Balanced Homologous translocation t(22q;22q) from father to a phenotypically normal daughter
D. K. Chopade, Harish Harde, Pallavi Ugale, Sandesh Chopade
January-March 2014, 20(1):85-88
DOI:10.4103/0971-6866.132765  PMID:24959022
  899 45 -
LETTER TO EDITOR
Glucose 6-phosphate dehydrogenase deficiency in Muslim community settled in Jaunpur district
Vandana Rai, Pradeep Kumar
January-March 2014, 20(1):96-97
DOI:10.4103/0971-6866.132770  PMID:24959025
  663 57 -
LETTERS TO EDITOR
ß-thalassemia and alkaptonuria
Sora Yasri, Viroj Wiwanitkit
January-March 2014, 20(1):97-97
DOI:10.4103/0971-6866.132772  PMID:24959026
  580 43 -
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