vol 25
Number VOL. 25 (1), 2022
12/28/2022
Front cover page: Front cover page: St. John the Evangelist, Church of the Mother of God “Hodegetria”, first half of the XIVth Century, Mušutište

Back cover page: Back cover page: PEARL, Amber bead, end of VI, beginning of V BC, Peter's Church, Novi Pazar
Cover design: Bitrakova-Grozdanova V, Skopje
A CASE OF MODY 2 - ASSOCIATED HYPERGLYCEMIA DIAGNOSED AS GESTATIONAL DIABETES
Chakarova N.1, Balabanski L.2,3, Dimova R.1, Tsarkova P.1, Tankova T.1
page: 4
DOUBLE ISOCHROMOSOME X, A RARE CYTOGENETIC VARIANT OF TURNER SYNDROME: A CASE REPORT AND A REVIEW OF THE LITERATURE
Zerrouki K.1,2, Babakhouya A.1,3, Tajir M.1,2
page: 4
APOE4 STATUS AND COGNITIVE FUNCTION IN MIDDLE-AGED AND ELDERLY PEOPLE
Pavel N.A.1, Paun M.R.2, Matei P.V.1,2, Dutu I.1, Tudose C.1,2
page: 6
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME WITH HETEROZYGOUS P.D50N IN THE GJB2 GENE IN TWO SERBIAN ADULT PATIENTS
Kalezić T.1,*, Vuković I.2, Stojković M.1, Stanojlović S.1, Karanović J.3, Brajušković G.3, Savić-Pavićević D.3
page: 6
A NOVEL VARIANT IN THE LIPA GENE ASSOCIATED WITH DISTINCT PHENOTYPE
Sarajlija A.1,6, Armengol L.2, Maver A.3, Kitic I.4,6, Prokic D.4,6, Cehic M.1, Djuricic M.S.5,7, Peterlin B.3
page: 8
A NOVEL LIKELY PATHOGENIC VARIANT IN THE RUNX1 GENE AS THE CAUSE OF CONGENITAL THROMBOCYTOPENIA
Despotović M1,*, Pereza N2, Peterlin B3, Ostojić S2, Golob B3, Maver A3, Roganović J4
page: 4
IDENTIFICATION OF KEY TARGET GENES AND PATHWAY ANALYSIS IN NONALCOHOLIC FATTY LIVER DISEASE VIA INTEGRATED BIOINFORMATICS ANALYSIS
Chen X.1, Zhang L.2, Wang Y.1, Li R.1, Yang M.1, Gao L.3*
page: 10
SINGLE NUCLEOTIDE POLYMORPHISMS IN IL-1A RS1800587, IL-1B RS1143634 AND VITAMIN D RECEPTOR RS731236 IN STAGE III GRADE B/C PERIODONTITIS
Özturk Özener H.1, Tacal Aslan B.2, Eken B.F.2, Agrali Ö.B.1, Yildrim H.S.1, Altunok E.Ç.3, Ulucan K.2, Kuru L.1
page: 10
COMPREHENSIVE GENETIC EVALUATION OF BULGARIAN CHILDREN WITH SYNDROMIC CRANIOSYNOSTOSIS
Delchev T.1, Hadjidekova S.2, Bichev S.3, Veleva Ts.1, Boneva I.4, Avdjieva-Tzavella D.1
page: 6
VITAMIN D RECEPTOR POLYMORPHISMS AMONG THE TURKISH POPULATION ARE ASSOCIATED WITH MULTIPLE SCLEROSIS
Bulan B1, Hoscan AY1, Keskin SN1, Cavus A1, Culcu EA1, Isik N2, List EO2, Arman A*4
page: 10
MOLECULAR CHARACTERIZATION OF MICRORNA INTERFERENCE AND ARISTOLOCHIC ACID INTOXICATION FOUND IN UPPER TRACT UROTHELIAL CARCINOMA IN PATIENTS WITH BALKAN ENDEMIC NEPHROPATHY: A SYSTEMATIC REVIEW OF THE CURRENT LITERATURE
Bašić D1*, Ignjatović I1, Janković Veličković Lj2, Veljković A3
page: 8
MATRIX METALLOPROTEINASE-2 (MMP-2 ) AND-9 (MMP-9) GENE VARIANTS AND MICROVASCULAR COMPLICATIONS IN TYPE 2 DIABETES PATIENTS
Andjelic Jelic M٭ˡ, Radojkovic D², Nikolic A², Rakicevic Lj², Babic T², Jelic D³, Lalic NM⁴
page: 6
“WE’VE OPENED PANDORA’S BOX, HAVEN’T WE?” CLINICAL GENETICISTS’ VIEWS ON ETHICAL ASPECTS OF GENOMIC TESTING IN NEONATAL INTENSIVE CARE
Arsov T.1,2
page: 8
MIR-147B REGULATED PROLIFERATION AND APOPTOSIS OF GASTRIC CANCER CELLS BY TARGETING CPEB2 VIA THE PTEN PATHWAY
Tao K.1,2, Dong J-H.2, Wang D.1, Li F.2†#, Zhang Z-T.#1*
page: 10



Number 27
VOL. 27 (1), 2024
Number 26
Number 26 VOL. 26(2), 2023 All in one
Number 26
VOL. 26(2), 2023
Number 26
VOL. 26, 2023 Supplement
Number 26
VOL. 26(1), 2023
Number 25
VOL. 25(2), 2022
Number 25
VOL. 25 (1), 2022
Number 24
VOL. 24(2), 2021
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VOL. 24(1), 2021
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VOL. 23(2), 2020
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VOL. 22(2), 2019
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VOL. 22(1), 2019
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VOL. 22, 2019 Supplement
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VOL. 21(2), 2018
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VOL. 21 (1), 2018
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VOL. 21, 2018 Supplement
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VOL. 20 (2), 2017
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VOL. 17 (1), 2014
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VOL. 16 (2), 2013
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VOL. 16 (1), 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.13 (1), 2010
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10 (1),2007
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1&2, 2006
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3&4, 2001
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Vol.3(2), 2000
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Number 1
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Number 1
Vol.2 (1), 1999
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Vol.1 (1), 1998

 

 


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