vol 24 Number VOL. 24(1), 2021 8/27/2021 Front cover page: Gold bracelet, unknown site, 4th century BC Back cover page: Bronze votive relief, Shala Albania, 2nd - 3th century AD Cover design: Bitrakova-Grozdanova V, Skopje TWO YEARS OF NEWBORN SCREENING FOR CYSTIC FIBROSIS IN NORTH MACEDONIA: FIRST EXPERIENCE Fustik S1,*, Anastasovska V2, Plaseska-Karanfilska D3, Stamatova A1, Spirevska L1, Pesevska M2, Terzikj M3, Vujovic M3 page: 41 A CASE OF GLYCOGEN STORAGE DISEASE TYPE 1a MIMICKING FAMILIAL CHYLOMICRONEMIA SYNDROME Olgac A1,*, Okur İ2, Biberoğlu G2, Ezgü FS2, Tümer L2 page: 103 SMITH-LEMLI-OPITZ SYNDROME: BOSNIAN AND HERZEGOVINIAN EXPERIENCE Begic N1,*, Begic Z1, Begic E2,3 page: 99 NOVEL MUTATION IN THE COL11A1 GENE CAUSING MARSHALL-STICKLER SYNDROME IN THREE GENERATIONS OF A BULGARIAN FAMILY Mladenova M1,2,*, Todorov T2, Grozdanova L3, Mitev V1, Todorova A1,2 page: 95 DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILY Pop-Jordanova N1,*, Zorcec T2, Sukarova-Angelovska E2, 3 page: 89 FAMILIAL ATYPICAL HEMOLYTIC UREMIC SYNDROME WITH POSITIVE p.S1191L (c.3572C>T) MUTATION ON THE CFH GENE: A SINGLE-CENTER EXPERIENCE Ersoy Dursun F1,*, Yesil G2, Sasak G3, Dursin H4 page: 81 GA GENOTYPE OF THE ARG280HIS POLYMORPHISM ON THE XRCC1 GENE: GENETIC SUSCEPTIBILITY GENOTYPE IN DIFFERENTIATED THYROID CARCINOMAS? Kirnap NG1,*, Tutuncu NB1,2, Yalcin Y2, Cebi HPB2, Tutuncu T2,3, Nar A1, Verdi H2, Atac FB2 page: 73 MUTATION STATUS AND IMMUNOHISTOCHEMICAL CORRELATION OF EGFR MUTATIONS IN GASTROINTESTINAL STROMAL TUMORS Ozkayalar H1, Ergoren MC2,3,*, Tuncel G2,3, Kurt S4, Cevik E4, Ozemri Sag S4, Yilmaz Ozguven B5, Kabukcuoglu F5, Mocan G1,2, Temel ŞG4,6,7,* page: 67 GENETIC ASSOCIATION OF SOLUTE CARRIER TRANSPORTER GENE VARIANTS WITH METFORMIN RESPONSE Abrahams-October Z1, Xhakaza L1, Pearce B1,*, Mandisa Masilela C1, Benjeddou M1, Vincent Adeniyi O2, Johnson R3,4, Jebio Ongole J5 page: 47 COMPARATIVE ANALYSIS OF GENES ASSOCIATED WITH OBESITY IN HUMANS USING BIOINFORMATIC DATA AND TOOLS Musliji ZS1, Pollozhani AK1, Lisichkov K2, Deligios M3, Popovski ZT2,4,* page: 35 DUAL EFFECT OF THE GHRL GENE VARIANT IN THE MOLECULAR PATHOGENESIS OF OBESITY Becer E1,2, Ergoren MC2,3,* page: 27 INCREASED EXPRESSION OF CARDIOTROPHIN-1 IN CARDIOMYOPATHY PATIENTS Sharif S1,*, Saleem A1, Naz S1, Rashid F1, Iqtedar M2, Kaleem A2, Latif A1 page: 21 ASSOCIATION OF NFKB1, NKX2-5, GATA4 AND RANKL GENE POLYMORPHISMS WITH SPORADIC CONGENITAL HEART DISEASE IN GREEK PATIENTS Aidinidou L1, Chatzikyriakidou A1, Giannopoulos A2, Karpa V1, Tzimou I2, Aidinidou E3, Fidani L1,* page: 15 PCSK9 GENE PARTICIPATES IN THE DEVELOPMENT OF PRIMARY DYSLIPIDEMIAS Matías-Pérez D1, Pérez-Santiago AD1, Sánchez Medina MA1, Alpuche Osorno JJ2, García-Montalvo IA1 page: 5 SIMULTANEOUSLY BOTH EXPRESSION OF LMP-1 AND METHYLATION OF E-CADHERIN: MOLECULAR BIOMARKER IN STAGE IV OF NASOPHARYNGEAL CARCINOMA PATIENTS Lao TD1, Truong PK1, Thieu HH1, Nguyen DH2, Nguyen MT3, Le TAH1,* page: 57

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