vol 20 Number VOL. 20 (2), 2017 2/8/2018 Front cover page: FEMALE STATUE, Stone, Belgrade (Singidunum), 3rd century A. D., National Museum, Belgrade Back cover page: MEDALION OF GORDIAN III, Bronze, 241–243 A. D., National Museum, Belgrade Cover design: Bitrakova-Grozdanova V, Skopje THE MITOCHONDRIAL COI/tRNASER(UCN) G7444A MUTATION MAY BE ASSOCIATED WITH HEARING IMPAIRMENT IN A HAN CHINESE FAMILY Ding Y1,2, Xia B-H3, Teng Y-S2,4, Zhuo G-C1,2, Leng J-H1,2,* page: 43 GALACTOSIALIDOSIS IN A NEWBORN WITH A NOVEL MUTATION IN THE CTSA GENE PRESENTING WITH TRANSIENT HYPERPARATHYROIDISM Okulu E1,*, Tunc G1, Eminoglu T2, Erdeve O1, Atasay B1, Arsan S1 page: 95 FEMALE AND MALE CARRIERS OF TAZ MUTATIONS NEED TO BE THOROUGHLY INVESTIGATED Finsterer J*, Stollberger C page: 91 EPIDERMAL GROWTH FACTOR RECEPTOR MUTATION STATUS: DOES YOUNGER MEAN MORE FREQUENTLY MUTATED? Wójcik P1, Krawczyk P2, Chorostowska-Wynimko J3, Reszka K4, Duk K3, Muszczyńska-Bernhard B5, Pankowski J6, Wojas-Krawczyk K2, Czyżewicz G7, Ramlau R8, Skoczek M7, Grenda A2,*, Orłowski T3, Grodzki T9, Piwowar M10, Roszkowski-Śliż K3, Milanowski J2 page: 89 DETECTION OF ALLELIC VARIANTS OF THE POLE AND POLD1 GENES IN COLORECTAL CANCER PATIENTS Pätzold LA, Bērziņa D, Daneberga Z, Gardovskis J, Miklaševičs E* page: 83 DIFFERENTIAL EXPRESSION OF FGFRs SIGNALING PATHWAY COMPONENTS IN BLADDER CANCER: A STEP TOWARD PERSONALIZED MEDICINE Ousati Ashtiani Z1,2, Tavakkoly-Bazzaz J2,*, Salami SA3, Pourmand MR4, Mansouri F5,6, Mashahdi R1, Pourmand G1,* page: 75 SUPEROXIDE DISMUTASE 1 AND 2 GENE POLYMORPHISM IN TURKISH VITILIGO PATIENTS Tuna A1, Ozturk G1, Gerceker TB1, Karaca E2,*, Onay H2, Guvenc SM2, Cogulu O2 page: 67 INCREASED FREQUENCY OF MEFV GENES IN PATIENTS WITH EPIGASTRIC PAIN SYNDROME Coskun BD1, Kiraz A2, Sevinc E1, Baspinar O3, Cakmak E4 page: 51 POLYMORPHISM OF THE ADRB2 rs1042713 GENE IS NOT ASSOCIATED WITH SPONTANEOUS PRETERM BIRTH: ANALYSES IN A SLOVENIAN SAMPLE AND META ANALYSIS Peterlin A1, Maver A1, Jan Z2, Lovrecic L1, Tul N2, Peterlin B1 page: 35 ASSOCIATION BETWEEN OSTEOPROTEGERIN GENE POLYMORPHISMS AND RISK OF CORONARY ARTERY DISEASE: A SYSTEMATIC REVIEW AND META-ANALYSIS Jia P, Wu N, Jia D*, Sun Y* page: 27 MOLECULAR CHARACTERIZATION OF IRANIAN PATIENTS WITH INHERITED COAGULATION FACTOR VII DEFICIENCY Shahbazi S1,*, Mahdian R2, Karimi K3, Mashayekhi A1 page: 19 ASSOCIATION BETWEEN INHERITED THROMBOPHILIA IN PREGNANCY AND MICRONUCLEUS FREQUENCY IN PERIPHERAL BLOOD LYMPHOCYTES Šošić GM1,*, Jović N2,5, Rakić B3, Dimitrijević A2,4, Varjačić M2,5 page: 11 ASSOCIATION OF PLACENTA PREVIA WITH A HISTORY OF PREVIOUS CESARIAN DELIVERIES AND INDICATIONS FOR A POSSIBLE ROLE OF A GENETIC COMPONENT Matalliotakis M1,*, Velegrakis A1, Goulielmos GN2, Niraki E1, Patelarou AE3, Matalliotakis I1 page: 5 ASSOCIATION OF THE MMP7 –181A>G PROMOTER POLYMORPHISM WITH EARLY ONSET OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE Tacheva T1,*, Dimov D2, Anastasov A1, Zhelyazkova Y2, Kurzawski M3, Gulubova M4, Drozdzik M3, Vlaykova T1 page: 59

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