vol 21 Number VOL. 21 (1), 2018 9/19/2018 Front cover page: Chancel screen, first half of the 9th century, Monastery St. Anne, Regional Museum, Koper Back cover page: Strap end, beginning of the 5th century, Gradec nad Mihovim, National Museum, Ljubljana Cover design: Bitrakova-Grozdanova V, Skopje THE MITOCHONDRIAL tRNAGly T10003C MUTATION MAY NOT BE ASSOCIATED WITH DIABETES MELLITUS Yuan Q, Zhao ZG, Yuan HJ page: 53 MUTATION IN PHOSPHOLIPASE C, δ1 (PLCD1) GENE UNDERLIES HEREDITARY LEUKONYCHIA IN A PASHTUN FAMILY AND REVIEW OF THE LITERATURE Khan AK, Khan SA, Muhammad Na, Muhammad No, Ahmad J, Nawaz H, Nasir A, Farman S, Khan S page: 69 ACUTE PRE-B LYMPHOBLASTIC LEUKEMIA AND CONGENITAL ANOMALIES IN A CHILD WITH A DE NOVO 22q11.1q11.22 DUPLICATION Vaisvilas M, Dirse V, Aleksiuniene B, Tamuliene I, Cimbalistiene L, Utkus A, Rascon J page: 87 FLOATING-HARBOR SYNDROME: PRESENTATION OF THE FIRST ROMANIAN PATIENT WITH A SRCAP MUTATION AND REVIEW OF THE LITERATURE Budisteanu M, Bögershausen N, Papuc SM, Moosa S, Thoenes M, Riga D, Arghir A, Wollnik B page: 83 PROBLEMS OF UNKNOWN SIGNIFICANCE: COUNSELING IN THE ERA OF NEXT GENERATION SEQUENCING Fahrioğlu U page: 73 UGT1A1 (TA)n PROMOTER GENOTYPE: DIAGNOSTIC AND POPULATION PHARMACOGENETIC MARKER IN SERBIA Vukovic M, Radlovic N, Lekovic Z, Vucicevic K, Maric N, Kotur N, Gasic V, Ugrin M, Stojiljkovic M, Dokmanovic L, Zukic B, Pavlovic S page: 59 PPARγ GENE AND ATHEROSCLEROSIS: GENETIC POLYMORPHISMS, EPIGENETICS AND THERAPEUTIC IMPLICATIONS Grbić E, Peterlin A, Kunej T, Petrovič D page: 39 ADRB2 GENE POLYMORPHISMS AND SALBUTAMOL RESPONSIVENESS IN SERBIAN CHILDREN WITH ASTHMA Jovicic N, Babic T, Dragicevic S, Nestorovic B, Nikolic A page: 33 FAMILY HISTORY AS AN IMPORTANT FACTOR FOR STRATIFYING PARTICIPANTS IN GENETIC STUDIES OF MAJOR DEPRESSION Zalar B, Blatnik A, Maver A, Klemenc-Ketiš Z, Peterlin B page: 5 ASSOCIATION OF E-SELECTIN S128R POLYMORPHISM WITH HEREDITARY BREAST CARCINOMA SUSCEPTIBILITY IN TURKISH PATIENTS WITHOUT BRCA1/2 GERMLINE MUTATIONS Yararbas K, Atalay PB page: 27 ANALYSIS OF THE PPARD GENE EXPRESSION LEVEL CHANGES IN FOOTBALL PLAYERS IN RESPONSE TO THE TRAINING CYCLE Domańska-Senderowska D, Snochowska A, Szmigielska P, Jastrzębski Z, Jegier A, Kiszałkiewicz J, Dróbka K, Jastrzębska J, Pastuszak-Lewandoska D, Cięszczyk P, Maciejewska-Skrendo A, Zmijewski P, Brzeziańska-Lasota E page: 19 DETECTING EGFR MUTATIONS IN PATIENTS WITH NON-SMALL CELL LUNG CANCER Hammoudeh ZA, Antonova O, Staneva R, Nikolova D, Kyuchukov Y, Penev A, Mintchev T, Koleva V, Hadjidekova S, Toncheva D page: 13 HYPERINSULINISM-HYPERAMMONEMIA SYNDROME IN AN INFANT WITH SEIZURES Strajnar A1, Tansek MZ2, Podkrajsek KT3,4, Battelino T2,5, Groselj U page: 77 CLINICAL VARIABILITY IN TWO MACEDONIAN FAMILIES WITH ARTERIAL TORTUOSITY SYNDROME Kocova M, Kacarska R, Kuzevska-Maneva K, Prijic S, Lazareska M, Dordoni C, Ritelli M, Colombi M page: 47

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