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   Table of Contents
Coverpage
April-June 2013
Volume 19 | Issue 2
Page Nos. 123-275

Online since Monday, August 05, 2013

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EDITORIAL  

Molecular aberration studies in cases of idiopathic mental retardation: An update p. 123
Dhanjit Kumar Das
DOI:10.4103/0971-6866.116100  PMID:24019609
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REVIEW ARTICLE Top

Birth defects in India: Hidden truth, need for urgent attention p. 125
Rinku Sharma
DOI:10.4103/0971-6866.116101  PMID:24019610
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ORIGINAL ARTICLES Top

Children with isolated growth hormone deficiency: Empty sella versus normal sella p. 130
Nagwa Abdallah Ismail, Nermeen Salah Eldin Metwaly, Fatma Ahmed El-Moguy, Mona Hassan Hafez, Soha M. Abd El Dayem, Tarek Mohamed Farid
DOI:10.4103/0971-6866.116102  PMID:24019611
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Etiology and genetic factors in clefts of lip and/or palate reported at children's hospital, Lahore, Pakistan p. 136
Muhammad Yaqoob, Farrukh Mahmood, Ghazala Hanif, Saima Mansoor Bugvi, Muhammad Afzal Sheikh
DOI:10.4103/0971-6866.116103  PMID:24019612
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Analysis of cytotoxic T-lymphocyte-associated antigen-4 and MMP-9 genes' methylation and their expression profiles with risk of non-alcoholic fatty liver disease p. 144
Dor Mohammad Kordi Tamandani, Mohammad Hashemi, Sara Shafiepour
DOI:10.4103/0971-6866.116106  PMID:24019613
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Body composition in Egyptian Turner syndrome girls p. 150
Moushira Erfan Zaki, Hanan H Afifi
DOI:10.4103/0971-6866.116108  PMID:24019614
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Haptoglobin2-2 phenotype is an additional risk factor of retinopathy in type 2 diabetes mellitus p. 154
Mukund R Mogarekar, Mahesh H Hampe
DOI:10.4103/0971-6866.116111  PMID:24019615
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Measuring opportunity for natural selection: Adaptation among two linguistically cognate tribes inhabiting two eco-situations of North-East India p. 159
Maitreyee Sarma
DOI:10.4103/0971-6866.116113  PMID:24019616
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Multiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South India p. 165
Neetha John, Moka Rajasekhar, Katta Mohan Girisha, Podila Satya Venkata Narasimha Sharma, Puthiya Mundyat Gopinath
DOI:10.4103/0971-6866.116115  PMID:24019617
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Subtelomeric chromosomal rearrangements in a large cohort of unexplained intellectually disabled individuals in Indonesia: A clinical and molecular study p. 171
Farmaditya E. P. Mundhofir, Willy M Nillesen, Bregje W. M. Van Bon, Dominique Smeets, Rolph Pfundt, Gaby van de Ven-Schobers, Martina Ruiterkamp-Versteeg, Tri I Winarni, Ben C. J. Hamel, Helger G Yntema, Sultana M. H. Faradz
PMID:24019618
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Small ubiquitin-like modifier 4 M55V polymorphism is not associated with diabetic nephropathy in Iranian type 2 diabetes patients p. 179
Farhad Shahsavar, Mehrzad Jafarzadeh, Alireza Azargoon, Mehdi Hedayati, Behnam Asadifar
DOI:10.4103/0971-6866.116121  PMID:24019619
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Analysis of methionine synthase reductase polymorphism (A66G) in Indian Muslim population p. 183
Vandana Rai, Upendra Yadav, Pradeep Kumar, Sushil Kumar Yadav
DOI:10.4103/0971-6866.116123  PMID:24019620
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CD14 C-159T polymorphism and its association with chronic lung diseases: A pilot study on isocyanate exposed population of Central India p. 188
Protiti Bose, Rashmi Bathri, Sajal De, KK Maudar
DOI:10.4103/0971-6866.116124  PMID:24019621
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Association between pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections disease and tumor necrosis factor-α gene−308 g/a, −850 c/t polymorphisms in 4-12-year-old children in Adana/Turkey p. 196
H Umit Luleyap, Dilge Onatoglu, M Bertan Yilmaz, Davut Alptekin, Aysegul Y Tahiroglu, Salih Cetiner, Ayfer Pazarbasi, Ilker Unal, Ayse Avci, Gamze Comertpay
DOI:10.4103/0971-6866.116116  PMID:24019622
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Proteus syndrome: Clinical profile of six patients and review of literature Highly accessed article p. 202
Suresh Kumar Angurana, Renu Suthar Angurana, Inusha Panigrahi, Ram Kumar Marwaha
DOI:10.4103/0971-6866.116117  PMID:24019623
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Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh p. 207
Ajay F Christopher, Anita Kumari, Sunali Chaudhary, Sandhya Hora, Ziledar Ali, Satish C Agrawal
DOI:10.4103/0971-6866.116119  PMID:24019624
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Angiotensin II type 1 receptor A1166C gene polymorphism and essential hypertension in Calabar and Uyo cities, Nigeria p. 213
Mary Esien Kooffreh, Chiaka Ijeoma Anumudu, Roseline Duke, Elza Cletus Okpako, P Lava Kumar
DOI:10.4103/0971-6866.116120  PMID:24019625
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Human leukocyte antigen alleles, genotypes and haplotypes frequencies in renal transplant donors and recipients from West Central India p. 219
Jaina S Patel, Manisha M Patel, Prakash G Koringa, Tejas M Shah, Amrutlal K Patel, Ajai K Tripathi, Anila Mathew, Mohan M Rajapurkar, Chaitanya G Joshi
DOI:10.4103/0971-6866.116122  PMID:24019626
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The effect of FokI vitamin D receptor polymorphism on bone mineral density in Jordanian perimenopausal women p. 233
Raed M Kanan
DOI:10.4103/0971-6866.116125  PMID:24019627
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Association between PRO12ALA polymorphism of the PPAR-γ2 gene and type 2 diabetes mellitus in Iranian patients p. 239
Azadeh Motavallian, Sasan Andalib, Golnaz Vaseghi, Hamid Mirmohammad-Sadeghi, Masoud Amini
DOI:10.4103/0971-6866.116126  PMID:24019628
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Genetic and environmental effects on age at menarche, and its relationship with reproductive health in twins p. 245
Shayesteh Jahanfar, Munn-Sann Lye, Isthrinayagy S Krishnarajah
DOI:10.4103/0971-6866.116127  PMID:24019629
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Comparison of in-vitro and in-vivo response to fetal hemoglobin production and γ-mRNA expression by hydroxyurea in Hemoglobinopathies p. 251
Khushnooma Italia, Farah Jijina, Rashid Merchant, Suchitra Swaminathan, Anita Nadkarni, Maya Gupta, Kanjaksha Ghosh, Roshan Colah
PMID:24019630
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CASE REPORTS Top

Early diagnosis of co-existent ß-thalassemia and alkaptonuria p. 259
Moushumi Lodh, Joshi A Kerketta
DOI:10.4103/0971-6866.116104  PMID:24019631
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Derivative chromosome 11 in a child resulting from a complex rearrangement involving chromosomes 3, 6 and 11 in father: Significance of parental karyotyping p. 262
Prabhat Ranjan, Kundanbala Desai, Shailaja Gada Saxena
DOI:10.4103/0971-6866.116105  PMID:24019632
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A case of Kartagener's syndrome: Importance of early diagnosis and treatment p. 266
Sanjay Gupta, Kumud K Handa, Ravi R Kasliwal, Pankaj Bajpai
DOI:10.4103/0971-6866.116107  PMID:24019633
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Sclerosterosis (Truswell-Hansen disease) p. 270
S Deepak Amalnath, M Vivekanandan
DOI:10.4103/0971-6866.116109  PMID:24019634
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LETTERS TO THE EDITOR Top

Micro-RNAs in IVF outcome p. 273
Saeid Ghorbian, Ahmad Poursadegh Zonouzi
DOI:10.4103/0971-6866.116110  PMID:24019635
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Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals p. 273
Khalil Hamzi, Bréhima Diakité, Amal Tazzite, Sellama Nadifi
DOI:10.4103/0971-6866.116112  PMID:24019636
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Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations p. 274
Amal Tazzite, Hassan Jouhadi, Khalil Hamzi, Abdellatif Benider, Sellama Nadifi
DOI:10.4103/0971-6866.116114  PMID:24019637
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