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THE JOURNAL GRANTS TO USERS’ OPEN ACCESS ONLINE OF THE FULL TEXT FROM START OF PUBLICATION - YEAR 2001-ONWARDS
VOLUME 14 CONTENTS 2014 VOLUME 14, Number 1 MARCH 2014
Manpreet Kaur and Badaruddoza • Genetic Polymorphism of Five STR Markers among Four Groups of Punjabi Population in North-West Punjab, India 1-7 DOI: 10.31901/24566330.2014/14.01.01
Aleksandra SaLagacka, Marta Zebrowska, Agnieszka Jelen, Marek Mirowski and Ewa Balcerczak • Haplotype Analysis of TNFA Gene in Peptic Ulcer Patients 9-15 DOI: 10.31901/24566330.2014/14.01.02
James D. Doecke, Thierry T. Chekouo, Francesco Stingo and Kim-Anh Do • miRNA Target Gene Identification: Sourcing miRNA Target Gene Relationships for the Analyses of TCGA Illumina MiSeq and RNA-Seq Hiseq Platform Data 17-22 DOI: 10.31901/24566330.2014/14.01.03
Ling Pan, Yali Sun, Songchang Chen, Jing He and Chenming Xu • SNP Microarray Characterization and Genotype-Phenotype Analysis in a Patient with a Ring Chromosome 23-26 DOI: 10.31901/24566330.2014/14.01.04
Tayfun Akalin, Seminur Haznedaroglu, Mehmet Ali Ergun, Engin Tezcan, Arif Kaya, Abdurrahman Tufan, Mehmet Akif Oztürk and Berna Goker • MEFV Mutations and CYP3A4 Polymorphisms Do Not Predict “Colchicine Responsiveness” in Familial Mediterranean Fever 27-32 DOI: 10.31901/24566330.2014/14.01.05
Anindya Dasgupta, Ushasi Banerjee, Pranab Roy, Aparna Khan, Mrinalkanti Ghosh and Kanika M. Chowdhuri • Assessment of CYP 17 Gene Polymorphism in Subjects with Polycystic Ovarian Syndrome and Central Obesity in an Indian Subpopulation 33-41 DOI: 10.31901/24566330.2014/14.01.06
Aylin Zekioglu, Fethi Sirri Çam, Nevzat Mutlutürk, Afig Berdeli and Muzaffer Çolakoglu • Analysis of Physical Activity Intensity, Alexithymia, and the COMT Val 158 Met Gene Polymorphism 43-48 DOI: 10.31901/24566330.2014/14.01.07
Guide to Contributors 49-54
List of Members of the Editorial Board 55-58
VOLUME 14, Number 2 june 2014
Esra Guney, Elvan Iseri, Sezen Guntekin Ergun , Emriye Ferda Percin, Mehmet Ali Ergun, Ozhan Yalcin and Sahnur Sene • T102C and 1438 G/A Polymorphisms of the Serotonin 2A Receptor Gene in Etiology and Course of ADHD 59-66 DOI: 10.31901/24566330.2014/14.02.01
Yamini Pokale, Priya Bansal, Juilee Vedpathak, Snehal Kulkarni, Jaya Vyas and Varsha Vadera • Case Report: Opitz C Syndrome with a Rare Chromosomal Abnormality 67-71 DOI: 10.31901/24566330.2014/14.02.02
D. Somasundaram, S. Palaniswami, R. Vijayabhasker and V. Venkatesakumar • G-Band Chromosome Segmentation, Overlapped Chromosome Separation and Visible Band Calculation 73-81 DOI: 10.31901/24566330.2014/14.02.03
B. B. Ganguly and N. N. Kadam • Prenatal Diagnosis of Fetus with Short Limbs Caused by Three Abnormal Chromosomes Inherited from Parents 83-90 DOI: 10.31901/24566330.2014/14.02.04
Lina Bashour • The Role of Interleukin-1 Haplotype in the Association between Atherosclerosis and Periodontitis in a Syrian Population 91-100 DOI: 10.31901/24566330.2014/14.02.05
Ahmet Inanir, Abdullah Cenikli, Ercan Tural, Akin Tekcan, Sengul Tural, Duygu Cakil and Serbulent Yigit • Molecular Analysis of Genetic Variation in Angiotensin I-Converting Enzyme Gene in Turkish Athletes 101-105 DOI: 10.31901/24566330.2014/14.02.06
VOLUME 14, Number 3, 4 SEPTEMBER, DECEMBER 2014
G. Gandhi, Jasmine Naru, Maninder Kaur and Gurpreet Kaur • DNA and Chromosoma I Damage in Residents near a Mobile Phone Base Station 107-118 DOI: 10.31901/24566330.2014/14.03-04.01
Susmita Bag, Sudha Ramaiah and Anand Anbarasu • Network and Polymorphic Analysis of Obesity Candidate Gene-Plin1: A Bioinformatics Approach 119-129 DOI: 10.31901/24566330.2014/14.03-04.02
Serkan Dogan, Adna Asic, Imer Muhovic, Larisa Besic and Damir Marjanovic • Overview of the Genetic STR Clustering among Worldwide Human Populations 131-142 DOI: 10.31901/24566330.2014/14.03-04.03
Melek Yuce and Hasan Bagci • Analysis of TNFRSF1A Gene R92Q Mutation in Familial Mediterranean Fever 143-148 DOI: 10.31901/24566330.2014/14.03-04.04
Hande Ayraler Taner, Sahnur Sener, Sezen Güntekin Ergün, Mehmet Ali Ergün and Esra Güney • Analysis of GNAL Polymorphisms in Attention Deficit Hyperactivity Disorder 149-153 DOI: 10.31901/24566330.2014/14.03-04.05
Pankaj Gadhia, Parita Balar, Tanvi Gonawala, Nitisha Parekh, Rachna Patel and Salil Vaniawala • Cytogenetic Study of Turner Syndrome and Its Variants 155-159 DOI: 10.31901/24566330.2014/14.03-04.06
Nguyen Thi Hue, Le Ngoc Yen and Tran Bao Ngoc • The Relationship between the Mutation rs3741378 of SIPA1 Gene and Breast Cancer in Vietnamese Women 161-168 DOI: 10.31901/24566330.2014/14.03-04.07
Ilhami Gok, Ozkan Ozta, Murat Celik and Cem Ozic • M694V and E148Q Mutations as Potential Molecular Markers for the Diagnosis of Familial Mediterranean Fever among Patients in the East Mediterranean Region of Turkey 169-175 DOI: 10.31901/24566330.2014/14.03-04.08
Ali Bayram, Feridun Akkafa, Ahmet Ozer and Remzi Yigiter • Decreased HDAC1 Gene Expression in Patients with Alzheimer’s Disease: A Study 177-182 DOI: 10.31901/24566330.2014/14.03-04.09
Sefa Senol, Ilker Akar, Kürsat Kargün, Ali Bayram, Murat Kara and Özlem Secen • Endothelin-1 Gene Polymorphism in Preoperative Myocardial Infarction with /or without Coronary Artery Bypass Graft 183-187 DOI: 10.31901/24566330.2014/14.03-04.10
Index 189-190
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