vol 23 Number VOL. 23(2), 2020 5/7/2021 Front cover page: Sarcophagus with Hippolythus and Phaedra, marble, Salona, Manastirine, early 4th century, AM, Split, Croatia. Back cover page: Mosaic fragment with a motif of Traditio legis, St. Maria Formosa, Pola, mid 6th century, AMI Pula, Croatia. Cover design: Bitrakova-Grozdanova V, Skopje CASE REPORT OF A SUCCESSFUL PREGNANCY IN A CYSTIC FIBROSIS PATIENT WITH THE c.1521_1523delCTT/c.3718-2477C>T GENOTYPES Spasova VL, Koleva LI, Toncheva DI, Karamisheva VI page: 103 TWO NOVEL CEBPA MUTATIONS IN A TURKISH PATIENT WITH ACUTE MYELOID LEUKEMIA Tokgun PE, Alay MT, Atli Tekin S, Güler N, Tokgun O, Demiray A, Karagenc N, Durak T, Celik B, Akca H page: 99 BILATERAL RENAL ANGIOMYOLIPOMAS AND SUBEPENDYMAL GIANT CELL ASTROCYTOMA ASSOCIATED WITH TUBEROUS SCLEROSIS COMPLEX: A CASE REPORT AND REVIEW OF THE LITERATURE Rambabova Bushljetik I, Lazareska M, Barbov I, Stankov O, Filipce V, Spasovski G page: 93 FAMILIAL NON-AUTOIMMUNE HYPERTHYROIDISM IN FAMILY MEMBERS ACROSS FOUR GENERATIONS DUE TO A NOVEL DISEASE-CAUSING VARIANT IN THE THYROTROPIN RECEPTOR GENE Malej A, Avbelj Stefanija M, Bratanič N, Trebušak Podkrajšek K, page: 87 FETAL CYSTIC HYGROMA ASSOCIATED WITH TERMINAL 2p25.1 DUPLICATION AND TERMINAL 3p25.3 DELETION: CYTOGENETIC, FLUORESCENT IN SITU HYBRIDIZATION AND MICROARRAY FAMILIAL CHARACTERIZATION OF TWO DIFFERENT CHROMOSOMAL STRUCTURAL REARRANGEMENTS Stipoljev F, Barbalic M, Logara M, Vicic A, Vulic M, Zekic Tomas S, Gjergja Juraski R page: 79 OSTEOPETRORICKETS IN AN INFANT WITH COEXISTENT CONGENITAL CYTOMEGALOVIRUS INFECTION Katsafiloudi M, Gombakis N, Hatzipantelis E, Tragiannidis A page: 107 EVALUATION OF METHYLATION PROFILES OF AN EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN A HEAD AND NECK SQUAMOUS CELL CARCINOMA PATIENT GROUP Mutlu M, Mutlu P, Azarkan S, Bayır O, Ocal B, Saylam G, Korkmaz MH page: 65 PROS AND CONS FOR FLUORESCENT IN SITU HYBRIDIZATION, KARYOTYPING AND NEXT GENERATION SEQUENCING FOR DIAGNOSIS AND FOLLOW-UP OF MULTIPLE MYELOMA Ikbal Atli E, Gurkan H, Onur Kirkizlar H, Atli E, Demir S, Yalcintepe S, Kalkan R, Demir AM page: 59 GENETIC SPECTRUM OF NEONATAL DIABETES Kocova M page: 5 THE UTILITY OF WHOLE EXOME SEQUENCING IN DIAGNOSING PEDIATRIC NEUROLOGICAL DISORDERS Muthaffar OY page: 17 ARRAY-COMPARATIVE GENOMIC HYBRIDIZATION RESULTS IN CLINICALLY AFFECTED CASES WITH APPARENTLY BALANCED CHROMOSOMAL REARRANGEMENTS Satkin NB, Karaman B, Ergin S, Kayserili H, Kalelioglu IH, Has R, Yuksel A, Basaran S page: 25 DO WE USE METHYLATION OF NFATC1 AND FOS GENES AS A BIOMARKER FOR POSTMENOPAUSAL OSTEOPOROSIS? Kalkan R, Tosun O page: 35 INFLUENCE OF POTENTIAL GENE POLYMORPHISMS ON PROPOFOL DOSAGE REGIMEN IN PATIENTS UNDERGOING ABDOMINAL HYSTERECTOMY Ivanov E, Sterjev Z, Budic I, Nojkov J, Karadzova D, Sivevski A page: 41 INVESTIGATION OF THE RELATIONSHIP OF TNFRSF11A GENE POLYMORPHISMS WITH BREAST CANCER DEVELOPMENT AND METASTASIS RISK IN PATIENTS WITH BRCA1 OR BRCA2 PATHOGENIC VARIANTS LIVING IN THE TRAKYA REGION OF TURKEY Özdemir K, Gürkan H, Demir S, Atli E, Özen Y, Sezer A, Tunçbilek N, Çicin İ page: 49

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