Indian Journal of Human Genetics
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   2010| September-December  | Volume 16 | Issue 3  
    Online since November 30, 2010

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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
  13,658 87 2
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
  11,024 64 1
Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?
Khalil Hamzi, Afaf Ben Itto, Sanaa Nassereddine, Sellama Nadifi
September-December 2010, 16(3):172-174
DOI:10.4103/0971-6866.73417  PMID:21206709
  5,167 66 -
Congenital malformations at birth in Central India: A rural medical college hospital based data
Amar Taksande, Krishna Vilhekar, Pushpa Chaturvedi, Manish Jain
September-December 2010, 16(3):159-163
DOI:10.4103/0971-6866.73412  PMID:21206705
  4,123 144 13
Pharmacogenomics of pediatric asthma
Sarika Gupta, Shally Awasthi
September-December 2010, 16(3):111-118
DOI:10.4103/0971-6866.73398  PMID:21206697
  3,288 165 5
Bone age is the best predictor of growth response to recombinant human growth hormone in Turner's syndrome
Nagwa Abdallah Ismail, Nermeen Salah Eldin Metwaly, Fatma Ahmed El-Moguy, Mona Hassan Hafez, Soha M Abd El Dayem, Tarek Mohamed Farid
September-December 2010, 16(3):119-126
DOI:10.4103/0971-6866.73400  PMID:21206698
  3,052 51 -
Oculo-facio-cardio-dental syndrome in a girl and her mother
Sudha Rudrappa, Rajendra Kumar, GS Kumar
September-December 2010, 16(3):169-171
DOI:10.4103/0971-6866.73416  PMID:21206708
  2,557 74 3
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India
Malay B Mukherjee, Anita H Nadkarni, Ajit C Gorakshakar, Kanjaksha Ghosh, Dipika Mohanty, Roshan B Colah
September-December 2010, 16(3):154-158
DOI:10.4103/0971-6866.73410  PMID:21206704
  2,116 148 7
Methionine synthase polymorphisms (MTR 2756 A>G and MTR 2758 C>G) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of Jordan
Helmi Yousif Al Farra
September-December 2010, 16(3):138-143
DOI:10.4103/0971-6866.73405  PMID:21206701
  2,095 63 11
Complexities and similarities of HLA antigen distribution in Asian subcontinent
U Shankarkumar
September-December 2010, 16(3):108-110
DOI:10.4103/0971-6866.73397  PMID:21206696
  2,009 133 2
The NQO1 allelic frequency in hindu population of central India varies from that of other Asian populations
Sher S Parihar, UK Chauhan
September-December 2010, 16(3):133-137
DOI:10.4103/0971-6866.73403  PMID:21206700
  2,060 63 1
Molecular analysis of human leukocyte antigen class I and class II allele frequencies and haplotype distribution in Pakistani population
T Moatter, M Aban, S Tabassum, U Shaikh, S Pervez
September-December 2010, 16(3):149-153
DOI:10.4103/0971-6866.73408  PMID:21206703
  2,008 67 8
Genetic assessment of serological and biochemical markers in Bharia tribe of Chhindwara district of Madhya Pradesh
Ruchira Chaudhary, Gunjan Sharma
September-December 2010, 16(3):127-132
DOI:10.4103/0971-6866.73401  PMID:21206699
  1,818 74 -
Defining genetic architecture of the populations in the Indian subcontinent: Impact of human leukocyte antigen diversity studies
NK Mehra
September-December 2010, 16(3):105-107
DOI:10.4103/0971-6866.73394  PMID:21206695
  1,712 173 6
Caspase 8 gene variants in healthy North Indian population and comparison with worldwide ethnic group variations
Ginu P George, Rama D Mittal
September-December 2010, 16(3):144-148
DOI:10.4103/0971-6866.73406  PMID:21206702
  1,413 56 -
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