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   2011| September-December  | Volume 17 | Issue 3  
    Online since January 20, 2012

 
 
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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
  6,122 18 1
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
  4,263 144 2
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
  3,607 56 12
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
  3,369 42 3
REVIEW ARTICLES
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
  3,287 56 -
ORIGINAL ARTICLES
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
  2,996 95 5
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 -
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
  2,927 48 3
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
  2,859 68 8
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
  2,565 113 5
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
  2,549 80 10
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
  2,544 83 3
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 -
LETTERS TO THE EDITOR
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
  2,370 32 -
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 -
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 -
CASE REPORTS
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
  2,231 54 1
ORIGINAL ARTICLES
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 -
CASE REPORTS
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
  2,181 23 1
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
  2,030 51 2
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
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 -
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 -
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
  1,731 31 1
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
  1,703 32 -
CASE REPORTS
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 -
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 -
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 -
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