Indian Journal of Human Genetics
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   Table of Contents
Coverpage
January-April 2012
Volume 18 | Issue 1
Page Nos. 1-138

Online since Saturday, May 26, 2012

Accessed 62,293 times.

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EDITORIAL  

Explaining anthropometric variations in sickle cell disease requires a multidimensional approach p. 1
Malay B Mukherjee, Kanjaksha Ghosh
DOI:10.4103/0971-6866.96632  
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COMMENTARY Top

Recollections of J.B.S. Haldane, with special reference to Human Genetics in India p. 3
Krishna R Dronamraju
DOI:10.4103/0971-6866.96634  
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REVIEW ARTICLES Top

Effect of gene polymorphisms on periodontal diseases p. 9
Fouzia Tarannum, Mohamed Faizuddin
DOI:10.4103/0971-6866.96638  
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Genetic biomarkers of depression p. 20
Anand Tamatam, Farhath Khanum, Amarinder Singh Bawa
DOI:10.4103/0971-6866.96639  
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Science of breeding and heredity from ancient Persia to modern Iran p. 34
Mohammad H Kariminejad, Ardeshir Khorshidian
DOI:10.4103/0971-6866.96641  
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ORIGINAL ARTICLES Top

An anthropometric and hematological comparison of sickle cell disease children from rural and urban areas p. 40
HS Nikhar, SU Meshram, GB Shinde
DOI:10.4103/0971-6866.96643  
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Prevalence of methylenetetrahydrofolate reductase C677T polymorphism in eastern Uttar Pradesh p. 43
Vandana Rai, Upendra Yadav, Pradeep Kumar
DOI:10.4103/0971-6866.96645  
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Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population p. 47
Rama D Mittal, Raju K Mandal
DOI:10.4103/0971-6866.96648  
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Epistatic interactions in idiopathic pulmonary arterial hypertension p. 56
Shivani Vadapalli, ML Satyanarayana, KL Chaitra, H Surekh Rani, B.K.S. Sastry, Pratibha Nallari
DOI:10.4103/0971-6866.96652  
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Molecular analysis of genetic variation in angiotensin I-converting enzyme identifies no association with sporting ability: First report from Indian population p. 62
Sweta T Kothari, Pratiksha Chheda, Leena Chatterjee, Bibhu R Das
DOI:10.4103/0971-6866.96653  
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Karyotypic findings in chronic myeloid leukemia cases undergoing treatment p. 66
Anupam Kaur, Simran Preet Kaur, Amarjit Singh, Jai Rup Singh
DOI:10.4103/0971-6866.96654  
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Inbreeding as a cause for deafness: Dadhkai study p. 71
Sushil Razdan, Sunil Kumar Raina, Kamal K Pandita, Shiveta Razdan, Renu Nanda, Rajni Kaul, Sandeep Dogra
DOI:10.4103/0971-6866.96655  
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Prenatal sonographic evaluation and postnatal outcome of renal anomalies p. 75
Manisha Kumar, Usha Gupta, Seema Thakur, Shilpi Aggrawal, Jyoti Meena, Sumedha Sharma, Shubha S Trivedi
DOI:10.4103/0971-6866.96656  
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In silico prediction of exposure amino acid sequences of outer inflammatory protein A of Helicobacter pylori for surface display on Eschierchia coli p. 83
Omid Teymournejad, Ashraf M Mobarez, Zuhair M Hassan, Seyed M Moazzeni, Bagher Yakhchali, Vajihe Eskandari
DOI:10.4103/0971-6866.96659  
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SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India p. 87
Edna D'Souza, Sona Nair, Anita Nadkarni, Kanjaksha Ghosh, Roshan B Colah
DOI:10.4103/0971-6866.96661  
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Utility of MLPA in mutation analysis and carrier detection for Duchenne muscular dystrophy p. 91
Prashant K Verma, Ashwin Dalal, Balraj Mittal, Shubha R Phadke
DOI:10.4103/0971-6866.96667  
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The effect of aging on micronuclei frequency and proliferation in human peripheral blood lymphocytes p. 95
Tuncay Orta, Süreyya Günebakan
DOI:10.4103/0971-6866.96671  
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Genetic sensitivity to bitter taste of 6-n Propylthiouracil: A useful diagnostic aid to detect early childhood caries in pre-school children p. 101
Raghavendra Pidamale, B Sowmya, Ann Thomas, Tony Jose
DOI:10.4103/0971-6866.96672  
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BRIEF REPORTS Top

Trisomy 8 in leukemia: A GCRI experience p. 106
Sonal R Bakshi, Manisha M Brahmbhatt, Pina J Trivedi, Esha N Dalal, Dharmesh M Patel, Sejal S Purani, Shilin N Shukla, Pankaj M Shah, Prabhudas S Patel
DOI:10.4103/0971-6866.96673  
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Recombination in human leukocyte antigen region in two Asian Indian families p. 109
Mahendra N Mishra, Ajay Sharma
DOI:10.4103/0971-6866.96674  
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CASE REPORTS Top

Cytogenetic investigation of patients with primary amenorrhea p. 112
K Vijaya Laxmi, SJ Babu, S Dayakar, RN Mehrothra, Kalal I Goud
DOI:10.4103/0971-6866.96676  
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Wolf-Hirschhorn syndrome: A case demonstrated by a cytogenetic study p. 117
Yamini S Pokale, Ajinkya M Jadhav, Ushang Kate
DOI:10.4103/0971-6866.96677  
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Familial germ cell tumor p. 119
Sanju Cyriac, Rejeev Rajendranath, A Robert Louis, TG Sagar
DOI:10.4103/0971-6866.96679  
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Methylenetetrahydrofolate reductase mutations, a genetic cause for familial recurrent neural tube defects p. 122
Laxmi V Yaliwal, Rathnamala M Desai
DOI:10.4103/0971-6866.96680  
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Cockayne syndrome-xeroderma pigmentosum complex with demyelination: A rare association p. 125
Usha Rani Singh, Shujaath Asif, Peter Prasanth Kumar Kommu, Philomina D'Souza
DOI:10.4103/0971-6866.96681  
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Dysmorphic features and congenital heart disease in chromosome 6q deletion: A short report p. 127
Sreelata Nair, Rini Varghese, Sajeed Hashim, Pappachan Scariah
DOI:10.4103/0971-6866.96682  
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A child with mosaicism for deletion (14)(q11.2q13) p. 130
Thilini H Gamage, Imaya U.H. Godapitiya, Shakila Nanayakkara, Rohan W Jayasekara, Vajira H.W. Dissanayake
DOI:10.4103/0971-6866.96684  
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A homozygous female hemophilia A p. 134
Preethi S Nair, S Shetty, Kanjaksha Ghosh
DOI:10.4103/0971-6866.96685  
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PERSONAL REFLECTION Top

A comparison of Fulani and Nadar HLA p. 137
Clyde Winters
DOI:10.4103/0971-6866.96686  
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