Indian Journal of Human Genetics
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   Table of Contents
Coverpage
September-December 2011
Volume 17 | Issue 3
Page Nos. 115-249

Online since Friday, January 20, 2012

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EDITORIALS  

Is RBC discrimination index suitable for differentiating between α- and β- thalassemias? p. 115
Ajit C Gorakshakar, Roshan B Colah
DOI:10.4103/0971-6866.92079  PMID:22345979
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Incidence of down syndrome: Hypotheses and reality Highly accessed article p. 117
Babu Rao Vundinti, Kanjaksha Ghosh
DOI:10.4103/0971-6866.92080  PMID:22345980
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REVIEW ARTICLES Top

Apoptosis and survival p. 120
Manjul Tiwari
DOI:10.4103/0971-6866.92081  PMID:22345981
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Neural tube defects between folate metabolism and genetics p. 126
Helmi Y Alfarra, Sabreen R Alfarra, Mai F Sadiq
DOI:10.4103/0971-6866.92082  PMID:22345982
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A comprehensive review on host genetic susceptibility to human papillomavirus infection and progression to cervical cancer p. 132
Koushik Chattopadhyay
DOI:10.4103/0971-6866.92087  PMID:22345983
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ORIGINAL ARTICLES Top

Evaluation of concentration and storage effects of mitomycin C in the diagnosis of Fanconi anemia among idiopatic aplastic anemia patients p. 145
H Mozdarani, K Abed Ashtiani, A Mohseni-Meybodi
DOI:10.4103/0971-6866.92088  PMID:22345984
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A six-nucleotide deletion polymorphism in the casp8 promoter is associated with reduced risk of esophageal and gastric cancers in Kashmir valley p. 152
Manzoor Ahmad Malik, Showkat Ali Zargar, Balraj Mittal
DOI:10.4103/0971-6866.92090  PMID:22345985
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Cytogenetic and comorbidity profile of Down syndrome in Mansoura University Children's Hospital, Egypt p. 157
Abdel-Hady El-Gilany, Sohier Yahia, Mohamed Shoker, Faeza El-Dahtory
DOI:10.4103/0971-6866.92092  PMID:22345986
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Genetic analysis of OCT1 gene polymorphisms in an Indian population p. 164
Gurusamy Umamaheswaran, Ramakrishnan G Praveen, Annan S Arunkumar, Ashok K Das, Deepak G Shewade, Chandrasekaran Adithan
DOI:10.4103/0971-6866.92094  PMID:22345987
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Haptoglobin polymorphism among the tribal groups of southern Gujarat p. 169
Priyanka Khurana, Aastha Aggarwal, Suraj Singh Huidrom, Gautam K Kshatriya
DOI:10.4103/0971-6866.92096  PMID:22345988
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Association of CYP3A5*3 polymorphism with development of acute leukemia p. 175
D Nageswara Rao, G Manjula, K Sailaja, D Surekha, D Raghunadharao, Senthil Rajappa, S Vishnupriya
DOI:10.4103/0971-6866.92098  PMID:22345989
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Evaluation of DNA damage in agricultural workers exposed to pesticides using single cell gel electrophoresis (comet) assay p. 179
Raminderjeet Kaur, Satbir Kaur, Mukesh Lata
DOI:10.4103/0971-6866.92100  PMID:22345990
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Tracing disease gene(s) in non-syndromic clefts of orofacial region: HLA haplotypic linkage by analyzing the microsatellite markers: MIB, C1_2_5, C1_4_1, and C1_2_A p. 188
R Rajendran, Saleem F Shaikh, Sukumaran Anil
DOI:10.4103/0971-6866.92101  PMID:22345991
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APOA1 gene polymorphisms in the South Asian immigrant population in the United States p. 194
Rebecca S Henkhaus, Sunita Dodani, Ann M Manzardo, Merlin G Butler
DOI:10.4103/0971-6866.92103  PMID:22345992
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Risk conferred by FokI polymorphism of vitamin D receptor (VDR) gene for essential hypertension p. 201
N Swapna, U Mohana Vamsi, G Usha, T Padma
DOI:10.4103/0971-6866.92104  PMID:22345993
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A comparative study of hematological parameters of α and β thalassemias in a high prevalence zone: Saudi Arabia p. 207
Syed Riaz Mehdi, Badr Abdullah Al Dahmash
DOI:10.4103/0971-6866.92106  PMID:22345994
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Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals p. 212
Khalil Hamzi, Amal Tazzite, Sellama Nadifi
DOI:10.4103/0971-6866.92105  PMID:22345995
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Growth response of Egyptian children with idiopathic short stature during four years of growth hormone therapy p. 218
Nagwa Abdallah Ismail, Nermeen Salah Eldin Metwaly, Fatma Ahmed El-Moguy, Mona Hassan Hafez, Soha M Abd El Dayem, Tarek Mohamed Farid
DOI:10.4103/0971-6866.92102  PMID:22345996
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CASE REPORTS Top

Refractory seizures with global developmental delay: A rare cause p. 226
PN Vinoth, Betty Chacko, J Julius Xavier Scott, Venkatasai
DOI:10.4103/0971-6866.92099  PMID:22345997
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Ross operation in a neuro-cardio-facial-cutaneous syndrome patient p. 229
Keyhan S Zanjani, Ali Akbar Zeinaloo, Hassan Radmehr
DOI:10.4103/0971-6866.92097  PMID:22345998
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A novel mutation (4040-4045 nt. delA) in exon 14 of the factor VIII gene causing severe hemophilia A p. 232
Habib Onsori, Mohammad Ali Hosseinpour Feizi, Abbas Ali Hosseinpour Feizi
DOI:10.4103/0971-6866.92095  PMID:22345999
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Acute promyelocytic leukemia with unusual karyotype p. 235
Mangala Gowri, SK Kousar Jahan, Kavitha , Prasannakumari , Madhumathi , L Appaji
DOI:10.4103/0971-6866.92093  PMID:22346000
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Octaploidy in idiopathic thrombocytopenic purpura p. 238
RN Makroo, Mohit Chowdhry, Manoj Mishra, Priyanka Srivastava, Ashish Fauzdar
DOI:10.4103/0971-6866.92091  PMID:22346001
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Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association p. 241
Jeevan M Kumar, Kalpana Gowrishankar, T Vasanthi, R Ashok Kumar, T Jayasudha
DOI:10.4103/0971-6866.92089  PMID:22346002
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LETTERS TO THE EDITOR Top

NQO1 C 609 T polymorphisms analyzed in a population from Kolkata, West Bengal p. 244
Sanjit Mukherjee, Keya Chaudhuri
DOI:10.4103/0971-6866.92083  PMID:22346003
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Hay-Wells syndrome of ectodermal dysplasia: A rare autosomal dominant disorder p. 245
NB Nagaveni, KV Umashankara
DOI:10.4103/0971-6866.92084  PMID:22346004
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Campomelic dysplasia p. 247
Jagdish P Goyal, Anshul Gupta, Vijay B Shah
DOI:10.4103/0971-6866.92085  PMID:22346005
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Null effect of p53 codon 72 polymorphism on recurrent pregnancy loss and recurrent implantation failure: A summative assessment p. 248
Viroj Wiwanitkit
DOI:10.4103/0971-6866.92086  PMID:22346006
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