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VOLUME 15                                        CONTENTS                                                        2015


VOLUME 15, Number 1                                                                                                                   MARCH  2015


 

INFORMATION ABOUT JOURNAL

 

I. Boronova, J. Bernasovska, G. Cakanova, P. Ferenc, E. Petrejcikova and V. Szabadosova • Heterochromatin Variants in Slovak Women with Reproductive Failure

1-5

DOI: 10.31901/24566330.2015/15.01.01

[Abstract] [Full Text - PDF]

 

Mehmet Ture, Tahsin Yakut, Adem Deligonul,  Mutlu Karkucak, Sebnem Ozemri Sag, Mustafa Hartavi, Erdem Cubukcu, Tuna Gulten and Turkkan Evrensel • Investigation of FGFR4 (Gly388Arg) Gene Polymorphism in Primary Lung Cancer Patients

7-12

DOI: 10.31901/24566330.2015/15.01.02

[Abstract] [Full Text - PDF] 

 

Bade Yamak, Melek Yuce, Hasan Bagci and Osman Imamoglu • Association between Sport Performance and  Alpha-Actinin-3 Gene R577X Polymorphism

13-19

DOI: 10.31901/24566330.2015/15.01.03

[Abstract] [Full Text - PDF]

 

Abir Ben Halima, Raoudha Bahri, Esther Esteban, Pedro Moral and Hassen Chaabani • Variation of Rhesus Haplotype Frequencies in North Africans and in Worldwide Population Analyses

21-31 

DOI: 10.31901/24566330.2015/15.01.04

[Abstract] [Full Text - PDF]

 

Birsen Baysal, Elcin Bora, Tufan Çankaya, Derya Erçal, Ayfer Ülgenalp, Sezin Canbek and Özlem Giray Bozkaya • Glutathione S-Transferase Gene Polymorphisms in Children with Down Syndrome and Their Mothers

33-39

DOI: 10.31901/24566330.2015/15.01.05

[Abstract] [Full Text - PDF]

 

Guide to Contributors

41-46

 

List of Members of the Editorial Board

47-49


VOLUME 15, Number 2                                                                                                           JUNE 2015


 

Bibhas Kar, S. Sivamani  and K. Sivakumar • Varying Clinical Presentation of Williams Syndrome:  A Case Series

51-54

DOI: 10.31901/24566330.2015/15.02.01

[Abstract] [Full Text - PDF]

 

Vasudeva Murthy, Lim Fuey Jia , Vijaya Paul Samuel,  and Kumaraswamy Kademane • Forensic Identification by Using Insertion-deletion Polymorphisms

55-59

DOI: 10.31901/24566330.2015/15.02.02

[Abstract] [Full Text - PDF]

 

Vasudeva Murthy.C.R.,Muhammad Zarif Asraf Bin Zulkeflle , Sunil Pazhayanur Venkateswaran  and Ankur Barua • Knowledge, Awareness and Participation of Medical and  Non-medical Students in the Malaysia National  Thalassemia Prevention Programme

61-72

DOI: 10.31901/24566330.2015/15.02.03

[Abstract] [Full Text - PDF]

 

Asker Zeki Ozsoy, Bulent Cakmak, Mehmet Can Nacar, Ali Cetin2, Fazli Demirturk,  Hatice Yilmaz Dogru, Nevin Karakus and Serbulent Yigit  • Mthfr and IL-4 Gene Polymorphisms Are Not Associated with Primary Dysmenorrhea in Young Adults

73-79

DOI: 10.31901/24566330.2015/15.02.04

[Abstract] [Full Text - PDF]

 

Krishnaveni and K. Prabhakaran • Alu Insertion/Deletion Polymorphism in Four Tribes of South India

81-87

DOI: 10.31901/24566330.2015/15.02.05

[Abstract] [Full Text - PDF]

 

Nagwa E. A. Gaboon  and Jumana Y. Al-Aama • Oro-Facio-Digital Syndrome Type IX with Polydactyly and Multiple Intraocular Findings

89-92

DOI: 10.31901/24566330.2015/15.02.06

[Abstract] [Full Text - PDF]

 


VOLUME 15, Number 3                                                                                                      SEPTEMBER 2015


 

Mutlu Karkucak , Berna Solak, Hakan Turan, Esma Uslu, Tahsin Yakut,  Cihangir bAliagaoglu and Teoman Erdem  •  MBL2 Gene Polymorphism and Risk of Vitiligo in Turkish Patients

93-96

DOI: 10.31901/24566330.2015/15.03.01

[Abstract] [Full Text - PDF]

 

Gursatej Gandhi and Gurpreet Kaur  •  Oxidative DNA Damage,  Oxidative Stress and Genetic Susceptibility- Prognostic Scores in ‘Missing’ COPD Cases

97-119

DOI: 10.31901/24566330.2015/15.03.02

[Abstract] [Full Text - PDF]

 

Melahat Kurtulus-Ulkuer, Uner Ulkuer and Ibrahim Baris  •  Evaluation of SNPs in the Mitochondrial DNA Using  NanoChip Microarrays in the Turkish Population

121-129

DOI: 10.31901/24566330.2015/15.03.03

[Abstract] [Full Text - PDF]

 

Tarnjeet Kaur, Annie Sodhi, Jatinder Singh, Sumeet Arora, Sukhdev Singh Kamboj and Manpreet Kaur  •  Evaluation of Galectin-3 Genetic Variants and its Serum Levels in Rheumatoid Arthritis in North India

131-138

DOI: 10.31901/24566330.2015/15.03.04

[Abstract] [Full Text - PDF]

 

Rana Al-Ajoury, Essam Kassem, Bassel Al-Halabi, Faten Moassess and Walid Al Achkar • Mutations Analysis of the Growth Differentiation Factor 9 Gene in Syrian Women with Ovarian Failure

139-144

DOI: 10.31901/24566330.2015/15.03.05

[Abstract] [Full Text - PDF]

 

Mehmet Cetinkaya, Mehmet Kaba, Esin Sakalli Cetin and Sukru Candan • Case Report: Y Chromosome Microdeletion in an Infertile Patient with Mosaic Klinefelter Syndrome

145-148

DOI: 10.31901/24566330.2015/15.03.06

[Abstract] [Full Text - PDF]

 

Prabha and Pooja Chadh • Risk Assessment of Occupational Exposure to Pesticides  among Pesticide Distributors of Punjab (India) Using Single Cell Gel Electrophoresis

149-155

DOI: 10.31901/24566330.2015/15.03.07

[Abstract] [Full Text - PDF]

 


VOLUME 15, Number 4                                                                                                    DECEMBER 2015


 

Aysun Baransel Isir, Abdulmuttalip Ozkorkmaz, Cesur Baransel, Ebru Gokalp Ozkorkmaz  and Sacide Pehlivan • Male Individualization Based on Y-Chromosomal Short Tandem Repeats: A Comparative Information Theoretical Analysis of 16 Y-STR Loci in Central Anatolia and Iraqi Populations

157-171

DOI: 10.31901/24566330.2015/15.04.01

[Abstract] [Full Text - PDF]

 

Gursatej Gandhi, Prabhjot Singh  and Gurpreet Kaur • Perspectives Revisited - The Buccal Cytome Assay  in Mobile Phone Users

173-182

DOI: 10.31901/24566330.2015/15.04.02

[Abstract] [Full Text - PDF]

 

Selma Yesilkaya, Mutlu Karkucak, Hikmet Coban, Ahmet Ursavas, Mehmet Ture and Tahsin Yakut • Angiotensin-Converting Enzyme Gene Insertion/Deletion Polymorphism in Patients with Pulmonary Thromboembolism

183-189

DOI: 10.31901/24566330.2015/15.04.03

[Abstract] [Full Text - PDF]

 

Worrawalan Lerttham, Goonnapa Fucharoen, Supawadee Yamsri and Supan Fucharoen • Two Independent Genetic Origins of b+-Thalassemia Due to -31 A to G Mutation in Thai and Japanese Populations

191-198

DOI: 10.31901/24566330.2015/15.04.04

[Abstract] [Full Text - PDF]

 

Sayee Rajangam, Preetha Tilak and Sonia Dhawan • Congenital Heart Defects and Chromosomal Abnormality

199-209

DOI: 10.31901/24566330.2015/15.04.05

[Abstract] [Full Text - PDF]

 

Index

211-213

[Full Text - PDF]