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, 241243 A. D., National Museum, Belgrade
Cover design: Bitrakova-Grozdanova V, Skopje
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
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
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
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
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
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
INCREASED FREQUENCY OF MEFV GENES IN PATIENTS WITH EPIGASTRIC PAIN SYNDROME
Coskun BD1, Kiraz A2, Sevinc E1, Baspinar O3, Cakmak E4
page: 51
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



Number 21
VOL. 21 (1), 2018
Number 21
VOL. 21, 2018 Accepted articles (Accepted, unedited articles, published online and can be cited. The final edited and printed version of the manuscript will appear in future)
Number 21
VOL. 21, 2018 Supplement
Number 20
VOL. 20 (2), 2017
Number 20
VOL. 20 (1), 2017
Number 19
VOL. 19 (2), 2016
Number 19
VOL. 19 (1), 2016
Number 18
VOL. 18 (2), 2015
Number 18
VOL. 18 (1), 2015
Number 17
VOL. 17 (2), 2014
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VOL. 17 (1), 2014
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VOL. 16 (2), 2013
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VOL. 15 (2), 2012
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VOL. 15, 2012 Supplement
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Vol. 15 (1), 2012
Number 14
14 - Vol. 14 (2), 2011
Number 14
The 9th Balkan Congress of Medical Genetics
Number 14
14 - Vol. 14 (1), 2011
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Vol. 13 (2), 2010
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Vol.2 (1), 1999
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