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   Table of Contents
Coverpage
September-December 2012
Volume 18 | Issue 3
Page Nos. 271-382

Online since Monday, March 04, 2013

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EDITORIALS  

Annoucement p. 271
Kanjaksha Ghosh
DOI:10.4103/0971-6866.107970  PMID:23716930
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Small players with a big role: MicroRNAs in pathophysiology of cleft lip and palate p. 272
Uppala Radhakrishna
DOI:10.4103/0971-6866.107973  PMID:23716931
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Vitamin D receptor and type 2 diabetes mellitus: Growing therapeutic opportunities p. 274
Parmeet Kaur Manchanda, Hemant K Bid
DOI:10.4103/0971-6866.107975  PMID:23716932
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REVIEW ARTICLE Top

Redefining the potential applications of dental stem cells: An asset for future p. 276
Shalu Rai, Mandeep Kaur, Sandeep Kaur, Sapna Panjwani Arora
DOI:10.4103/0971-6866.107976  PMID:23716933
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ORIGINAL ARTICLES Top

Evaluation of C677T polymorphism of the methylenetetra hydrofolate reductase gene and its association with levels of serum homocysteine, folate, and vitamin B12 as maternal risk factors for Down syndrome p. 285
Pankaj K Mohanty, Seema Kapoor, Anand P Dubey, Sanjeev Pandey, Renuka Shah, Hemant K Nayak, Sunil K Polipalli
DOI:10.4103/0971-6866.107977  PMID:23716934
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Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in Phenylketonuria patients in Western Iran p. 290
Keyvan Moradi, Reza Alibakhshi, Keyghobad Ghadiri, Saeid Reza Khatami, Hamid Galehdari
DOI:10.4103/0971-6866.107978  PMID:23716935
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Hemoglobinopathies in South Gujarat population and incidence of anemia in them p. 294
Ankur G Patel, Avani P Shah, Smita M Sorathiya, Snehalata C Gupte
DOI:10.4103/0971-6866.107979  PMID:23716936
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Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India p. 299
Shashikant Sharma, Tekcham Dinesh Singh, Satish S Poojary, Manoj Singh Rohilla, Ajaypal Singh, Kishore B Lowalekar, Pramod Kumar Tiwari
DOI:10.4103/0971-6866.107981  PMID:23716937
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The use of hormones indicators in human saliva in diagnosing parodontitis in pregnant women p. 305
SI Dolomatov, W Zukow, ID Atmazhov, R Muszkieta, A Skaliy
DOI:10.4103/0971-6866.107982  PMID:23716938
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Conditional deletion of the human ortholog gene Dicer1 in Pax2-Cre expression domain impairs orofacial development p. 310
Laura C Barritt, Joseph M Miller, Laura R Scheetz, Kelsey Gardner, Marsha L Pierce, Garrett A Soukup, Sonia M Rocha-Sanchez
DOI:10.4103/0971-6866.107984  PMID:23716939
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The low frequency of Y chromosome microdeletions in subfertile males in a Sinhalese population of Sri Lanka p. 320
Tithila Kalum Wettasinghe, Rohan W Jayasekara, Vajira H. W. Dissanayake
DOI:10.4103/0971-6866.107985  PMID:23716940
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Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriers p. 326
Risha Nahar, Renu Saxena, Roumi Deb, Ishwar C Verma
DOI:10.4103/0971-6866.107987  PMID:23716941
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Genetic significance of muscle segment homeo box1 gene in South Indian population for cleft lip and palate p. 332
S Prasad Venkanna, Venkatesh Shivani
DOI:10.4103/0971-6866.107988  PMID:23716942
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Analysis of loss of heterozygsity effect on thyroid tumor with oxyphilia cell locus in familial non medullary thyroid carcinoma in Iranian families p. 340
Hasti Atashi Shirazi, Mehdi Hedayati, Maryam Sadat Daneshpour, Abdollah Shafiee, Fereidoun Azizi
DOI:10.4103/0971-6866.107989  PMID:23716943
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BRIEF REPORT Top

Rhizomelic chondrodysplasia punctata: A missed opportunity for early diagnosis p. 344
Nanda Chhavi, Sankar Prashanth, Chandrasekaran Venkatesh, Kadirvel Karthikeyan
DOI:10.4103/0971-6866.107990  PMID:23716944
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CASE REPORTS Top

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type p. 346
Katta Mohan Girisha, Aroor Shrikiran, Abdul Mueed Bidchol, Osamu Sakamoto, Puthiya Mundyat Gopinath, Kapaettu Satyamoorthy
DOI:10.4103/0971-6866.108025  PMID:23716945
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An uncommon case of an adult with del(5)(q) in acute lymphoblastic leukemia p. 349
E Venkataswamy, Ashwini R Nargund, Shilpa Prabhudesai, Geeta V Patil, J Chandra Rao, Vidya H Veldore, Shekar Patil, Amit Verma, Rashmita Sahoo, BS Ajaikumar, Prasannakumari
DOI:10.4103/0971-6866.108028  PMID:23716946
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A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation Highly accessed article p. 352
Leon Mutesa, Mauricette Jamar, Anne Cecile Hellin, Genevieve Pierquin, Vincent Bours
DOI:10.4103/0971-6866.108033  PMID:23716947
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Proteus syndrome: A rare case report p. 356
Keerthi Talari, Praveen Kumar Arinaganhalli Subbanna, Deepak Amalnath, Subrahmanyam Dharanitragada Krishna Suri
DOI:10.4103/0971-6866.108036  PMID:23716948
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A case of oligoasthenoteratozoospermia with AZFc deletion and persistent oxidative stress p. 359
Rajender Singh, Ahmad Mohammad Kaleem, Sankhwar Satya Narayana, Abbas Ali Mahdi
DOI:10.4103/0971-6866.108037  PMID:23716949
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Renal amyloidosis due to familial Mediterranean fever misdiagnosed p. 363
Iman Hama, Ratbi Ilham, Naima Ouzeddoun, Zaitouna Alhamany, Radia Bayahia, Abdelaziz Sefiani
DOI:10.4103/0971-6866.108043  PMID:23716950
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A new syndrome with overlapping features of Townes-brocks syndrome and single median maxillary central incisor syndrome p. 366
Thirunavukkarasu Arun Babu, Venkatesh Chandrasekaran, Sathish Balachandran
DOI:10.4103/0971-6866.108047  PMID:23716951
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A novel 11;18 translocation in a case of acute myeloid leukemia with maturation p. 369
G Sandhya Devi, Faiq Ahmed, Kavita Khadke, Sudha S Murthy, Senthil J Rajappa
DOI:10.4103/0971-6866.108050  PMID:23716952
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Seven nipples in a male: World's second case report Highly accessed article p. 373
Tarang Goyal, SK Bakshi, Anupam Varshney
DOI:10.4103/0971-6866.108051  PMID:23716953
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Orofaciodigital syndrome type-VI (Varadi-Papp syndrome) with several Y-shaped metacarpals p. 376
Pulak R Mahato, Shashi B Pandey
DOI:10.4103/0971-6866.108053  PMID:23716954
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LETTERS TO THE EDITOR Top

Octaploidy in idiopathic thrombocytopenia purpura: Is it incidental or causal? p. 379
Shantashri Vaidya, Babu Rao Vundinti
DOI:10.4103/0971-6866.108055  PMID:23716955
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Chronic pancreatitis: A new pathophysiology p. 380
Shweta Singh, Ravindra Kumar, Gourdas Choudhuri, Sarita Agarwal
DOI:10.4103/0971-6866.108056  PMID:23716956
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