Indian Journal of Human Genetics
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  Most popular articles (Since February 01, 2006)

 
 
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ORIGINAL COMMUNICATIONS
Genetic damage in mobile phone users: some preliminary findings
Gursatej Gandhi, Anita
May-August 2005, 11(2):99-104
DOI:10.4103/0971-6866.16810  
  70,853 732 39
ORIGINAL ARTICLES
Identification of a rare blood group, "Bombay (Oh) phenotype," in Bhuyan tribe of Northwestern Orissa, India
RS Balgir
September-December 2007, 13(3):109-113
DOI:10.4103/0971-6866.38985  PMID:21957358
  28,016 418 4
ORIGINAL COMMUNICATIONS
Association of SP-D, MBL and I-NOS genetic variants with pulmonary tuberculosis
Mudit Vaid, Savneet Kaur, Madan Taruna, Hari Singh, Vijay K Gupta, KJR Murthy, Puranam U Sarma
September-December 2006, 12(3):105-110
DOI:10.4103/0971-6866.29851  
  24,814 250 1
Pericentric inversion of chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases
Babu V Rao, Lily Kerketta, Seema Korgaonkar, Kanjaksha Ghosh
September-December 2006, 12(3):129-132
DOI:10.4103/0971-6866.29856  
  23,514 714 13
CASE REPORTS
Triploidy in a fetus following amniocentesis referred for maternal serum screening test at second trimester
E Bagherizadeh, M Oveisi, Z Hadipour, A Saremi, Y Shafaghati, F Behjati
May-August 2010, 16(2):94-96
DOI:10.4103/0971-6866.69371  PMID:21031058
  23,181 80 -
ORIGINAL ARTICLE
Impact of pericentric inversion of Chromosome 9 [inv (9) (p11q12)] on infertility
Hossein Mozdarani, Anahita Mohseni Meybodi, Hamideh Karimi
January-April 2007, 13(1):26-29
DOI:10.4103/0971-6866.32031  PMID:21957338
  17,724 564 10
CASE REPORTS
A Sri Lankan child with 49,XXXXY syndrome
Vajira H.W Dissanayake, Palinda Bandarage, Christeen R.J Pedurupillay, Rohan W Jayasekara
September-December 2010, 16(3):164-165
DOI:10.4103/0971-6866.73413  PMID:21206706
  15,140 92 2
REVIEW ARTICLE
Connexin 26 and autosomal recessive non-syndromic hearing loss
Monisha Mukherjee, SR Phadke, Balraj Mittal
July-December 2003, 9(2):40-50
  14,047 339 -
Contribution of genomics, proteomics, and single-nucleotide polymorphism in toxicology research and Indian scenario
S Patel, D Parmar, YK Gupta, MP Singh
May-August 2005, 11(2):61-75
DOI:10.4103/0971-6866.16804  
  12,569 687 5
CASE REPORTS
A rare case of congenital heart disease with ambiguous genitalia
Kusuma Lingaiah, Bharath A Parshwanath, Savitha R Mysore, Balasundaram Krishnamurthy, Nallur B Ramachandra
September-December 2010, 16(3):166-168
DOI:10.4103/0971-6866.73414  PMID:21206707
  12,684 67 1
ORIGINAL COMMUNICATIONS
Menstrual history in women with down syndrome - A review
Priya Ranganath, Sayee Rajangam
January-June 2004, 10(1):18-21
  11,509 187 -
BRIEF REPORT
Chromosome 12;15 rearrangements in patients with recurrent miscarriage
SB Nair, G Mukundan, BM Paul, L Ramachandran, KK Gopinathan, Sajayan Joseph
September-December 2006, 12(3):133-139
DOI:10.4103/0971-6866.29857  
  11,055 362 -
CASE REPORTS
Facio-auricular vertebral syndrome-a case report
M V. V. Reddy, PP Reddy, P Usha Rani, L Hema Bindu
September-December 2005, 11(3):156-158
DOI:10.4103/0971-6866.19537  
  10,844 255 5
ORIGINAL COMMUNICATIONS
Prevalence of congenital heart diseases in Mysore
R Smitha, SC Karat, D Narayanappa, B Krishnamurthy, SN Prasanth, NB Ramachandra
January-April 2006, 12(1):11-16
DOI:10.4103/0971-6866.25296  
  10,331 434 17
Heterozygosity and allele frequencies of the two VNTRs (ApoB and D1S80) in Iranian population
Nejat Mahdieh, Elham Tafsiri, Morteza Karimipour, Mohammad T Akbari
January-June 2005, 11(1):31-34
DOI:10.4103/0971-6866.16292  
  10,054 666 7
Molecular characterization of mutations causing β -thalassemia in Faisalabad Pakistan using the amplification refractory mutation system (ARMS-PCR)
Shahid M Baig, F Rabbi, U Hameed, JA Qureshi, Z Mahmood, SH Bokhari, A Kiani, H Hassan, JM Baig, A Azhar, T Zaman
May-August 2005, 11(2):80-83
DOI:10.4103/0971-6866.16806  
  10,035 552 7
REVIEW ARTICLE
Stem cells: A new paradigm
Sachin Kumar, NP Singh
January-April 2006, 12(1):4-10
DOI:10.4103/0971-6866.25295  
  9,389 791 -
CASE REPORTS
TRISOMY 18 in a 50-year-old female
B Bhanumathi, Neelam A Goyel, ZA Mishra
September-December 2006, 12(3):146-147
DOI:10.4103/0971-6866.29860  
  9,691 174 7
REVIEW ARTICLE
Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran
Rahim Fakher, Kaeikhaei Bijan, Akbari Mohammad Taghi
January-April 2007, 13(1):5-15
DOI:10.4103/0971-6866.32028  PMID:21957335
  8,943 760 11
REVIEW ARTICLES
DNA profiling: Social, legal, or biological parentage
AK Sharma
September-December 2007, 13(3):88-92
DOI:10.4103/0971-6866.38981  PMID:21957354
  8,730 448 2
REVIEW ARTICLE
An understanding the genetic basis of congenital heart disease
Smitha Ramegowda, Nallur B Ramachandra
January-June 2005, 11(1):14-23
DOI:10.4103/0971-6866.16289  
  8,608 533 6
ORIGINAL ARTICLE
Detection of Y STR markers of male fetal dna in maternal circulation
Seema P Nair, Sam Peter, VV Pillay, UM Remya, R Krishnaprasad, B Rajammal
May-August 2007, 13(2):69-72
DOI:10.4103/0971-6866.34710  PMID:21957349
  8,786 326 -
SHORT COMMUNICATION
Genetic heterogeneity of population structure in 15 major scheduled tribes in central-eastern India: A study of immuno-hematological disorders
RS Balgir
May-August 2006, 12(2):86-92
DOI:10.4103/0971-6866.27792  
  8,593 367 7
REVIEW ARTICLE
The impact of consanguinity on the Indian population
AH Bittles
July-December 2002, 8(2):45-51
  8,449 462 12
Past, present and future perspectives of genetic therapy in gliomas
Tobias Alécio Mattei, Ricardo Ramina, Marcos Tatagiba, Paulo Henrique Aguiar
January-June 2005, 11(1):4-13
DOI:10.4103/0971-6866.16288  
  8,185 238 -
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