Indian Journal of Human Genetics
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   Table of Contents
Coverpage
July-September 2013
Volume 19 | Issue 3
Page Nos. 277-378

Online since Wednesday, October 30, 2013

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EDITORIAL  

Warfarin pharmacogenetics: How close are we to clinical practice? p. 277
Tejasvita Gaikwad, Shrimati Shetty, Kanjaksha Ghosh
DOI:10.4103/0971-6866.120806  PMID:24339537
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REVIEW ARTICLES Top

Hemoglobin E disorder: Newborn screening program p. 279
Viroj Wiwanitkit
DOI:10.4103/0971-6866.120808  PMID:24339538
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An overview of gene therapy in head and neck cancer p. 282
Amit Bali, Deepika Bali, Ashutosh Sharma
DOI:10.4103/0971-6866.120811  PMID:24339539
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ORIGINAL ARTICLES Top

Usage of U7 small nuclear ribonucleic acid in gene therapy of hemoglobin D Punjab disorder: Rationale? p. 291
Viroj Wiwanitkit
DOI:10.4103/0971-6866.120812  PMID:24339540
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Polymorphism at P21 codon 31 and dinucleotide polymorphism of P73 gene and susceptibility to bladder cancer in individuals from North India p. 293
Praveen Kumar Jaiswal, Vibha Singh, Rama Devi Mittal
DOI:10.4103/0971-6866.120815  PMID:24339541
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Inter and intra ethnic variation of vitamin K epoxide reductase complex and cytochrome P450 4F2 genetic polymorphisms and their prevalence in South Indian population p. 301
Dhakchinamoorthi Krishna Kumar, Deepak Gopal Shewade, Sajjanavar Manjunath, Prayaga Ushakiran, Gangadharan Reneega, Chandrasekaran Adithan
DOI:10.4103/0971-6866.120817  PMID:24339542
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Phenotypic spectrum in uniparental disomy: Low incidence or lack of study? p. 311
Arpan D Bhatt, Thomas Liehr, Sonal R Bakshi
DOI:10.4103/0971-6866.120819  PMID:24339543
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Index of opportunity for natural selection among the Gowdas of Kodagahalli village, Karnataka, India p. 315
Bhaboklang Sohkhlet
DOI:10.4103/0971-6866.120821  PMID:24339544
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No CAG repeat expansion of polymerase gamma is associated with male infertility in Tamil Nadu, South India p. 320
J Poongothai
DOI:10.4103/0971-6866.120823  PMID:24339545
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Linkage study of DFNB3 responsible for hearing loss in human p. 325
Akhtar Ali, Masroor E Babar, Saeeda Kalsoom, Jamil Ahmad, Kamran Abbas
DOI:10.4103/0971-6866.120827  PMID:24339546
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Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss p. 331
Majida Charif, Redouane Boulouiz, Amina Bakhechane, Houda Benrahma, Halima Nahili, Abdelmajid Eloualid, Hassan Rouba, Mostafa Kandil, Omar Abidi, Guy Lenaers, Abdelhamid Barakat
DOI:10.4103/0971-6866.120828  PMID:24339547
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Analysis of hemoglobin electrophoresis results and physicians investigative practices in Saudi Arabia p. 337
Syed Riaz Mehdi, Badr Abdullah Al Dahmash
DOI:10.4103/0971-6866.120829  PMID:24339548
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Population based family history analysis of Brahmins in a small town in India for the prevalence of type-2 diabetes mellitus p. 342
Arun V Panat, Dilip A Kulkarni, Ravindra B Ghooi
DOI:10.4103/0971-6866.120826  PMID:24339549
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CASE REPORTS Top

Mosaic double aneuploidy: Down syndrome and XYY p. 346
Mayur Parihar, Beena Koshy, Vivi Miriam Srivastava
DOI:10.4103/0971-6866.120825  PMID:24339550
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Poland syndrome a rare congenital anomaly p. 349
Aliyu Ibrahim, Abdallah Ramatu, Akhiwu Helen
DOI:10.4103/0971-6866.120824  PMID:24339551
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Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India p. 352
Ranjeet Singh Mashon, Sona Nair, Pratibha Sawant, Roshan B Colah, Kanjaksha Ghosh, Sheila Das
DOI:10.4103/0971-6866.120822  PMID:24339552
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Genetic analysis of a family with complete androgen insensitivity syndrome p. 355
Sunil Kumar Kota, Kotni Gayatri, Siva Krishna Kota, Sruti Jammula
DOI:10.4103/0971-6866.120820  PMID:24339553
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Type 2 diabetes mellitus: An unusual association with Down's syndrome p. 358
Sunil Kumar Kota, Prabhas Ranjan Tripathy, Siva Krishna Kota, Sruti Jammula
DOI:10.4103/0971-6866.120818  PMID:24339554
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A case of primary amenorrhea with 46+XY genotype from Kashmir Valley p. 360
Shahid Mudassir Baba, Aga Syed Sameer, Mushtaq A Siddiqi
DOI:10.4103/0971-6866.120816  PMID:24339555
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Hypoparathyroidism-retardation-dysmorphism syndrome p. 363
Kalenahalli Jagadish Kumar, Halasahalli Chowdegowda Krishna Kumar, Vadambal Gopalakrishna Manjunath, Sangaraju Mamatha
DOI:10.4103/0971-6866.120814  PMID:24339556
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A novel ABCB11 mutation in an Iranian girl with progressive familial intrahepatic cholestasis p. 366
Sassan Saber, Reza Vazifehmand, Iman Bagherizadeh, Mahbubeh Kasiri
DOI:10.4103/0971-6866.120813  PMID:24339557
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Genetic mutations in Gorlin-Goltz syndrome p. 369
Muthumula Daneswari, Mutjumula Swamy Ranga Reddy
DOI:10.4103/0971-6866.120810  PMID:24339558
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Novel three missense mutations observed in Von Hippel-Lindau gene in a patient reported with renal cell carcinoma p. 373
Pasupuleti Santhosh Kumar, Katari Venkatesh, Lokanathan Srikanth, Potukuchi Venkata Gurunadha Krishna Sarma, Akkamgari Ramprasad Reddy, Srinivasan Subramanian, Bobbidi Venkata Phaneendra
DOI:10.4103/0971-6866.120809  PMID:24339559
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LETTER TO THE EDITOR Top

Possible impact of factor V Leiden genotype on warfarin induced bleeding p. 377
Tejasvita Gaikwad, Kanjaksha Ghosh, Shrimati Shetty
DOI:10.4103/0971-6866.120807  PMID:24339560
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