Indian Journal of Human Genetics
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   Table of Contents
Coverpage
January-March 2014
Volume 20 | Issue 1
Page Nos. 1-97

Online since Monday, May 19, 2014

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EDITORIAL  

Familial Mediterranean fever: An unusual disease enlightening the inflammation biology p. 1
Kanjaksha Ghosh, Ajit C Gorakshakar
DOI:10.4103/0971-6866.132741  PMID:24959007
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REVIEW ARTICLE Top

Genes and oral cancer p. 4
Sunit Kumar Jurel, Durga Shanker Gupta, Raghuwar D. Singh, Mrinalini Singh, Shilpi Srivastava
DOI:10.4103/0971-6866.132745  PMID:24959008
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Reactive metabolites and antioxidant gene polymorphisms in type 2 diabetes mellitus Highly accessed article p. 10
Monisha Banerjee, Pushpank Vats
DOI:10.4103/0971-6866.132747  PMID:24959009
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Neurotransmitters in alcoholism: A review of neurobiological and genetic studies p. 20
Niladri Banerjee
DOI:10.4103/0971-6866.132750  PMID:24959010
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ORIGINAL ARTICLES Top

Pattern of chromosome involvement in childhood hyperdiploid pre-B-cell acute lymhoblastic leukemia cases from India p. 32
Lily S. Kerketta, Vundinti Baburao, Kanjaksha Ghosh
DOI:10.4103/0971-6866.132751  PMID:24959011
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Association study of the ABCC8 gene variants with type 2 diabetes in south Indians p. 37
Radha Venkatesan, Dhanasekaran Bodhini, Nagarajan Narayani, Viswanathan Mohan
DOI:10.4103/0971-6866.132752  PMID:24959012
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Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children' Hospital, Mansoura, Egypt p. 43
Mohammad S. Al-Haggar, Sohier Yahia, Dina Abdel-Hady, Afaf Al-Saied, Rasha Al-Kenawy, Rabab Abo-El-Kasem
DOI:10.4103/0971-6866.132755  PMID:24959013
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Paraoxonase1, its Q192R polymorphism and HDL-cholesterol in relation to intensive cardiac care unit stay in ischemic heart disease p. 51
Mahesh Harishchandra Hampe, Mukund Ramchandra Mogarekar
DOI:10.4103/0971-6866.132756  PMID:24959014
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Association of single nucleotide polymorphisms of CACNA1A gene in migraine p. 59
Aadil Bashir, Shiekh Saleem, Maqbool Wani, Roohi Rasool, Irfan Yousuf Wani, Azhara Gulnar, Sawan Verma
DOI:10.4103/0971-6866.132757  PMID:24959015
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A comprehensive analysis of breakpoint cluster region-abelson fusion oncogene splice variants in chronic myeloid leukemia and their correlation with disease biology p. 64
Zafar Iqbal
DOI:10.4103/0971-6866.132758  PMID:24959016
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CASE REPORTS Top

Chronic myeloid leukemia in case of Klinefelter syndrome p. 69
Vasundhara Chennuri, Rajesh Kashyap, Parag Tamhankar, Subha Phadke
DOI:10.4103/0971-6866.132760  PMID:24959017
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Raine syndrome p. 72
B. Vishwanath, K. Srinivasa, M. Veera Shankar
DOI:10.4103/0971-6866.132761  PMID:24959018
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Berardinelli-Seip syndrome type 1 in an Egyptian child p. 75
Kotb Abbass Metwalley, Hekma Saad Farghaly
DOI:10.4103/0971-6866.132762  PMID:24959019
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A novel chromosomal abnormality t (9;14)(p24;q13) in B-acute lymphoblastic leukemia p. 79
Sureshkumar Raveendran, Santhi Sarojam, Geetha Narayanan, Hariharan Sreedharan
DOI:10.4103/0971-6866.132763  PMID:24959020
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Poland syndrome p. 82
Chandra Madhur Sharma, Shrawan Kumar, Manoj K. Meghwani, Ravi P. Agrawal
DOI:10.4103/0971-6866.132764  PMID:24959021
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Unexpected Inheritance of a Balanced Homologous translocation t(22q;22q) from father to a phenotypically normal daughter p. 85
D. K. Chopade, Harish Harde, Pallavi Ugale, Sandesh Chopade
DOI:10.4103/0971-6866.132765  PMID:24959022
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Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies p. 89
Abdelhafid Natiq, Siham Chafai Elalaoui, Thomas Liehr, Saïd Amzazi, Abdelaziz Sefiani
DOI:10.4103/0971-6866.132767  PMID:24959023
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BRIEF REPORTS Top

Split-hand/feet malformation in three tamilian families and review of the reports from India p. 92
S. Deepak Amalnath, Maya Gopalakrishnan, Tarun Kumar Dutta
DOI:10.4103/0971-6866.132769  PMID:24959024
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LETTER TO EDITOR Top

Glucose 6-phosphate dehydrogenase deficiency in Muslim community settled in Jaunpur district p. 96
Vandana Rai, Pradeep Kumar
DOI:10.4103/0971-6866.132770  PMID:24959025
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LETTERS TO EDITOR Top

ß-thalassemia and alkaptonuria p. 97
Sora Yasri, Viroj Wiwanitkit
DOI:10.4103/0971-6866.132772  PMID:24959026
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