Indian Journal of Human Genetics
Home Current Issue Archives Guidelines Subscriptions e-Alerts Reader Login
Users online: 119
Print this page  Email this page Small font sizeDefault font sizeIncrease font size
Export selected to
Endnote
Reference Manager
Procite
Medlars Format
RefWorks Format
BibTex Format
  Citation statistics : Table of Contents
   2011| September-December  | Volume 17 | Issue 3  
    Online since January 20, 2012

 
 
  Archives   Previous Issue   Next Issue   Most popular articles   Most cited articles
 
Show all abstracts  Show selected abstracts  Export selected to
  Cited Viewed PDF
ORIGINAL ARTICLES
Risk conferred by FokI polymorphism of vitamin D receptor (VDR) gene for essential hypertension
N Swapna, U Mohana Vamsi, G Usha, T Padma
September-December 2011, 17(3):201-206
DOI:10.4103/0971-6866.92104  PMID:22345993
  12 3,608 56
Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals
Khalil Hamzi, Amal Tazzite, Sellama Nadifi
September-December 2011, 17(3):212-217
DOI:10.4103/0971-6866.92105  PMID:22345995
  10 2,550 80
REVIEW ARTICLES
A comprehensive review on host genetic susceptibility to human papillomavirus infection and progression to cervical cancer
Koushik Chattopadhyay
September-December 2011, 17(3):132-144
DOI:10.4103/0971-6866.92087  PMID:22345983
  8 2,859 68
ORIGINAL ARTICLES
Genetic analysis of OCT1 gene polymorphisms in an Indian population
Gurusamy Umamaheswaran, Ramakrishnan G Praveen, Annan S Arunkumar, Ashok K Das, Deepak G Shewade, Chandrasekaran Adithan
September-December 2011, 17(3):164-168
DOI:10.4103/0971-6866.92094  PMID:22345987
  5 2,565 113
Evaluation of DNA damage in agricultural workers exposed to pesticides using single cell gel electrophoresis (comet) assay
Raminderjeet Kaur, Satbir Kaur, Mukesh Lata
September-December 2011, 17(3):179-187
DOI:10.4103/0971-6866.92100  PMID:22345990
  5 2,996 95
CASE REPORTS
Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association
Jeevan M Kumar, Kalpana Gowrishankar, T Vasanthi, R Ashok Kumar, T Jayasudha
September-December 2011, 17(3):241-243
DOI:10.4103/0971-6866.92089  PMID:22346002
  3 3,370 42
ORIGINAL ARTICLES
A comparative study of hematological parameters of α and β thalassemias in a high prevalence zone: Saudi Arabia
Syed Riaz Mehdi, Badr Abdullah Al Dahmash
September-December 2011, 17(3):207-211
DOI:10.4103/0971-6866.92106  PMID:22345994
  3 2,544 83
Cytogenetic and comorbidity profile of Down syndrome in Mansoura University Children's Hospital, Egypt
Abdel-Hady El-Gilany, Sohier Yahia, Mohamed Shoker, Faeza El-Dahtory
September-December 2011, 17(3):157-163
DOI:10.4103/0971-6866.92092  PMID:22345986
  3 2,928 48
EDITORIALS
Incidence of down syndrome: Hypotheses and reality
Babu Rao Vundinti, Kanjaksha Ghosh
September-December 2011, 17(3):117-119
DOI:10.4103/0971-6866.92080  PMID:22345980
  2 4,265 144
ORIGINAL ARTICLES
Association of CYP3A5*3 polymorphism with development of acute leukemia
D Nageswara Rao, G Manjula, K Sailaja, D Surekha, D Raghunadharao, Senthil Rajappa, S Vishnupriya
September-December 2011, 17(3):175-178
DOI:10.4103/0971-6866.92098  PMID:22345989
  2 2,030 51
CASE REPORTS
A novel mutation (4040-4045 nt. delA) in exon 14 of the factor VIII gene causing severe hemophilia A
Habib Onsori, Mohammad Ali Hosseinpour Feizi, Abbas Ali Hosseinpour Feizi
September-December 2011, 17(3):232-234
DOI:10.4103/0971-6866.92095  PMID:22345999
  1 6,123 18
Acute promyelocytic leukemia with unusual karyotype
Mangala Gowri, SK Kousar Jahan, Kavitha , Prasannakumari , Madhumathi , L Appaji
September-December 2011, 17(3):235-237
DOI:10.4103/0971-6866.92093  PMID:22346000
  1 2,231 54
Octaploidy in idiopathic thrombocytopenic purpura
RN Makroo, Mohit Chowdhry, Manoj Mishra, Priyanka Srivastava, Ashish Fauzdar
September-December 2011, 17(3):238-240
DOI:10.4103/0971-6866.92091  PMID:22346001
  1 2,182 23
ORIGINAL ARTICLES
APOA1 gene polymorphisms in the South Asian immigrant population in the United States
Rebecca S Henkhaus, Sunita Dodani, Ann M Manzardo, Merlin G Butler
September-December 2011, 17(3):194-200
DOI:10.4103/0971-6866.92103  PMID:22345992
  1 1,732 31
CASE REPORTS
Refractory seizures with global developmental delay: A rare cause
PN Vinoth, Betty Chacko, J Julius Xavier Scott, Venkatasai
September-December 2011, 17(3):226-228
DOI:10.4103/0971-6866.92099  PMID:22345997
  - 1,883 29
Ross operation in a neuro-cardio-facial-cutaneous syndrome patient
Keyhan S Zanjani, Ali Akbar Zeinaloo, Hassan Radmehr
September-December 2011, 17(3):229-231
DOI:10.4103/0971-6866.92097  PMID:22345998
  - 1,666 16
EDITORIALS
Is RBC discrimination index suitable for differentiating between α- and β- thalassemias?
Ajit C Gorakshakar, Roshan B Colah
September-December 2011, 17(3):115-116
DOI:10.4103/0971-6866.92079  PMID:22345979
  - 1,853 111
LETTERS TO THE EDITOR
NQO1 C 609 T polymorphisms analyzed in a population from Kolkata, West Bengal
Sanjit Mukherjee, Keya Chaudhuri
September-December 2011, 17(3):244-245
DOI:10.4103/0971-6866.92083  PMID:22346003
  - 1,220 48
Hay-Wells syndrome of ectodermal dysplasia: A rare autosomal dominant disorder
NB Nagaveni, KV Umashankara
September-December 2011, 17(3):245-246
DOI:10.4103/0971-6866.92084  PMID:22346004
  - 2,371 32
Campomelic dysplasia
Jagdish P Goyal, Anshul Gupta, Vijay B Shah
September-December 2011, 17(3):247-248
DOI:10.4103/0971-6866.92085  PMID:22346005
  - 1,924 37
Null effect of p53 codon 72 polymorphism on recurrent pregnancy loss and recurrent implantation failure: A summative assessment
Viroj Wiwanitkit
September-December 2011, 17(3):248-249
DOI:10.4103/0971-6866.92086  PMID:22346006
  - 972 28
ORIGINAL ARTICLES
Haptoglobin polymorphism among the tribal groups of southern Gujarat
Priyanka Khurana, Aastha Aggarwal, Suraj Singh Huidrom, Gautam K Kshatriya
September-December 2011, 17(3):169-174
DOI:10.4103/0971-6866.92096  PMID:22345988
  - 2,309 78
Evaluation of concentration and storage effects of mitomycin C in the diagnosis of Fanconi anemia among idiopatic aplastic anemia patients
H Mozdarani, K Abed Ashtiani, A Mohseni-Meybodi
September-December 2011, 17(3):145-151
DOI:10.4103/0971-6866.92088  PMID:22345984
  - 2,969 42
A six-nucleotide deletion polymorphism in the casp8 promoter is associated with reduced risk of esophageal and gastric cancers in Kashmir valley
Manzoor Ahmad Malik, Showkat Ali Zargar, Balraj Mittal
September-December 2011, 17(3):152-156
DOI:10.4103/0971-6866.92090  PMID:22345985
  - 2,219 49
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
R Rajendran, Saleem F Shaikh, Sukumaran Anil
September-December 2011, 17(3):188-193
DOI:10.4103/0971-6866.92101  PMID:22345991
  - 1,704 32
Growth response of Egyptian children with idiopathic short stature during four years of growth hormone therapy
Nagwa Abdallah Ismail, Nermeen Salah Eldin Metwaly, Fatma Ahmed El-Moguy, Mona Hassan Hafez, Soha M Abd El Dayem, Tarek Mohamed Farid
September-December 2011, 17(3):218-225
DOI:10.4103/0971-6866.92102  PMID:22345996
  - 2,463 19
REVIEW ARTICLES
Apoptosis and survival
Manjul Tiwari
September-December 2011, 17(3):120-125
DOI:10.4103/0971-6866.92081  PMID:22345981
  - 2,273 77
Neural tube defects between folate metabolism and genetics
Helmi Y Alfarra, Sabreen R Alfarra, Mai F Sadiq
September-December 2011, 17(3):126-131
DOI:10.4103/0971-6866.92082  PMID:22345982
  - 3,289 56
  Search 
  The Journal 
  The Association 
  Site Statistics 
  Addresses 
  My Preferences 
  Online Submission