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  Citation statistics : Table of Contents
   2012| September-December  | Volume 18 | Issue 3  
    Online since March 4, 2013

 
 
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EDITORIALS
Vitamin D receptor and type 2 diabetes mellitus: Growing therapeutic opportunities
Parmeet Kaur Manchanda, Hemant K Bid
September-December 2012, 18(3):274-275
DOI:10.4103/0971-6866.107975  PMID:23716932
  2 1,591 78
ORIGINAL ARTICLES
Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriers
Risha Nahar, Renu Saxena, Roumi Deb, Ishwar C Verma
September-December 2012, 18(3):326-331
DOI:10.4103/0971-6866.107987  PMID:23716941
  2 1,556 34
CASE REPORTS
A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation
Leon Mutesa, Mauricette Jamar, Anne Cecile Hellin, Genevieve Pierquin, Vincent Bours
September-December 2012, 18(3):352-355
DOI:10.4103/0971-6866.108033  PMID:23716947
  1 6,192 39
A case of oligoasthenoteratozoospermia with AZFc deletion and persistent oxidative stress
Rajender Singh, Ahmad Mohammad Kaleem, Sankhwar Satya Narayana, Abbas Ali Mahdi
September-December 2012, 18(3):359-362
DOI:10.4103/0971-6866.108037  PMID:23716949
  1 1,685 47
Orofaciodigital syndrome type-VI (Varadi-Papp syndrome) with several Y-shaped metacarpals
Pulak R Mahato, Shashi B Pandey
September-December 2012, 18(3):376-378
DOI:10.4103/0971-6866.108053  PMID:23716954
  1 2,389 29
EDITORIALS
Small players with a big role: MicroRNAs in pathophysiology of cleft lip and palate
Uppala Radhakrishna
September-December 2012, 18(3):272-273
DOI:10.4103/0971-6866.107973  PMID:23716931
  1 1,416 57
ORIGINAL ARTICLES
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
Pankaj K Mohanty, Seema Kapoor, Anand P Dubey, Sanjeev Pandey, Renuka Shah, Hemant K Nayak, Sunil K Polipalli
September-December 2012, 18(3):285-289
DOI:10.4103/0971-6866.107977  PMID:23716934
  1 1,459 81
Hemoglobinopathies in South Gujarat population and incidence of anemia in them
Ankur G Patel, Avani P Shah, Smita M Sorathiya, Snehalata C Gupte
September-December 2012, 18(3):294-298
DOI:10.4103/0971-6866.107979  PMID:23716936
  1 3,243 87
Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India
Shashikant Sharma, Tekcham Dinesh Singh, Satish S Poojary, Manoj Singh Rohilla, Ajaypal Singh, Kishore B Lowalekar, Pramod Kumar Tiwari
September-December 2012, 18(3):299-304
DOI:10.4103/0971-6866.107981  PMID:23716937
  1 2,605 70
Conditional deletion of the human ortholog gene Dicer1 in Pax2-Cre expression domain impairs orofacial development
Laura C Barritt, Joseph M Miller, Laura R Scheetz, Kelsey Gardner, Marsha L Pierce, Garrett A Soukup, Sonia M Rocha-Sanchez
September-December 2012, 18(3):310-319
DOI:10.4103/0971-6866.107984  PMID:23716939
  1 2,496 28
REVIEW ARTICLE
Redefining the potential applications of dental stem cells: An asset for future
Shalu Rai, Mandeep Kaur, Sandeep Kaur, Sapna Panjwani Arora
September-December 2012, 18(3):276-284
DOI:10.4103/0971-6866.107976  PMID:23716933
  1 2,657 130
BRIEF REPORT
Rhizomelic chondrodysplasia punctata: A missed opportunity for early diagnosis
Nanda Chhavi, Sankar Prashanth, Chandrasekaran Venkatesh, Kadirvel Karthikeyan
September-December 2012, 18(3):344-345
DOI:10.4103/0971-6866.107990  PMID:23716944
  - 1,492 35
CASE REPORTS
Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type
Katta Mohan Girisha, Aroor Shrikiran, Abdul Mueed Bidchol, Osamu Sakamoto, Puthiya Mundyat Gopinath, Kapaettu Satyamoorthy
September-December 2012, 18(3):346-348
DOI:10.4103/0971-6866.108025  PMID:23716945
  - 1,523 44
An uncommon case of an adult with del(5)(q) in acute lymphoblastic leukemia
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
September-December 2012, 18(3):349-351
DOI:10.4103/0971-6866.108028  PMID:23716946
  - 1,241 36
Proteus syndrome: A rare case report
Keerthi Talari, Praveen Kumar Arinaganhalli Subbanna, Deepak Amalnath, Subrahmanyam Dharanitragada Krishna Suri
September-December 2012, 18(3):356-358
DOI:10.4103/0971-6866.108036  PMID:23716948
  - 1,586 45
Renal amyloidosis due to familial Mediterranean fever misdiagnosed
Iman Hama, Ratbi Ilham, Naima Ouzeddoun, Zaitouna Alhamany, Radia Bayahia, Abdelaziz Sefiani
September-December 2012, 18(3):363-365
DOI:10.4103/0971-6866.108043  PMID:23716950
  - 1,209 19
A new syndrome with overlapping features of Townes-brocks syndrome and single median maxillary central incisor syndrome
Thirunavukkarasu Arun Babu, Venkatesh Chandrasekaran, Sathish Balachandran
September-December 2012, 18(3):366-368
DOI:10.4103/0971-6866.108047  PMID:23716951
  - 1,499 25
A novel 11;18 translocation in a case of acute myeloid leukemia with maturation
G Sandhya Devi, Faiq Ahmed, Kavita Khadke, Sudha S Murthy, Senthil J Rajappa
September-December 2012, 18(3):369-372
DOI:10.4103/0971-6866.108050  PMID:23716952
  - 1,612 36
Seven nipples in a male: World's second case report
Tarang Goyal, SK Bakshi, Anupam Varshney
September-December 2012, 18(3):373-375
DOI:10.4103/0971-6866.108051  PMID:23716953
  - 5,096 36
EDITORIALS
Annoucement
Kanjaksha Ghosh
September-December 2012, 18(3):271-271
DOI:10.4103/0971-6866.107970  PMID:23716930
  - 1,261 76
LETTERS TO THE EDITOR
Octaploidy in idiopathic thrombocytopenia purpura: Is it incidental or causal?
Shantashri Vaidya, Babu Rao Vundinti
September-December 2012, 18(3):379-379
DOI:10.4103/0971-6866.108055  PMID:23716955
  - 733 23
Chronic pancreatitis: A new pathophysiology
Shweta Singh, Ravindra Kumar, Gourdas Choudhuri, Sarita Agarwal
September-December 2012, 18(3):380-382
DOI:10.4103/0971-6866.108056  PMID:23716956
  - 1,024 37
ORIGINAL ARTICLES
The use of hormones indicators in human saliva in diagnosing parodontitis in pregnant women
SI Dolomatov, W Zukow, ID Atmazhov, R Muszkieta, A Skaliy
September-December 2012, 18(3):305-309
DOI:10.4103/0971-6866.107982  PMID:23716938
  - 1,540 40
Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in Phenylketonuria patients in Western Iran
Keyvan Moradi, Reza Alibakhshi, Keyghobad Ghadiri, Saeid Reza Khatami, Hamid Galehdari
September-December 2012, 18(3):290-293
DOI:10.4103/0971-6866.107978  PMID:23716935
  - 1,490 35
The low frequency of Y chromosome microdeletions in subfertile males in a Sinhalese population of Sri Lanka
Tithila Kalum Wettasinghe, Rohan W Jayasekara, Vajira H. W. Dissanayake
September-December 2012, 18(3):320-325
DOI:10.4103/0971-6866.107985  PMID:23716940
  - 1,513 39
Genetic significance of muscle segment homeo box1 gene in South Indian population for cleft lip and palate
S Prasad Venkanna, Venkatesh Shivani
September-December 2012, 18(3):332-339
DOI:10.4103/0971-6866.107988  PMID:23716942
  - 1,321 45
Analysis of loss of heterozygsity effect on thyroid tumor with oxyphilia cell locus in familial non medullary thyroid carcinoma in Iranian families
Hasti Atashi Shirazi, Mehdi Hedayati, Maryam Sadat Daneshpour, Abdollah Shafiee, Fereidoun Azizi
September-December 2012, 18(3):340-343
DOI:10.4103/0971-6866.107989  PMID:23716943
  - 1,307 21
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