vol 13 Number Vol.13 (1), 2010 5/14/2010 Front cover page: Portrait in bronze of a Byzantine empress. Balajnac, 5th or 6th century A.D. National Museum in Nis, Serbia Back cover page: Jupiter on a throne, a bronze statue. Nis, 1st century A.D. National Museum in Nis, Serbia Cover design: Bitrakova-Grozdanova V, Skopje, Republic of Macedonia DE NOVO DUPLICATION OF CHROMOSOME 7 (q21.1-q32); CASE REPORT AND REVIEW OF THE LITERATURE Nasiri F1, Mahjoubi F1,2,*, Babamohammadi G1 page: 37 CHROMATIN QUALITY AS A CRUCIAL FACTOR FOR THE SUCCESS OF FLUORESCENT IN SITU HYBRIDIZATION ANALYSES OF UNFERTILIZED OOCYTES, POLAR BODIES AND ARRESTED ZYGOTES Zhivkova RS1,*, Delimitreva SM1, Toncheva DI2, Vatev IT1 page: 3 Possible association of maternal haemorrhoid with congenital abnormalities in their children – a population-based case-control study Ferenc Bánhidy, M.D.1, Nándor Ács, M.D.1, Erzsébet H. Puhó2, and Andrew E. Czeizel2* page: 25 A PARTIAL TRISOMY 2p(p21->pter) DERIVED FROM A PATERNAL t(2;4)(p21;q33) KARYOTYPE Mahjoubi F1,*, Zolfagary N2 page: 41 UNIQUE PRESENTATION OF AN 8p DELETION IN A DISCORDANT TWIN WITH ATRIOVENTRICULAR CANAL DEFECT AND PROLONGED HYPOGLYCEMIA Kumar P*, Elshershari H, Parashette KR, Ize-Ludlow D, Harris C page: 47 TRISOMY 21 WITH A SMALL SUPERNUMERARY MARKER CHROMOSOME DERIVED FROM CHROMOSOMES 13/21 AND 18 Niksic SB1, Deretic VI2, Pilic GR1, Ewers E3, Merkas M3, Ziegler M3, Liehr T3,* page: 57 A p.P30L MUTATION AT THE CYP21A2 GENE IN MACEDONIAN PATIENTS WITH NONCLASSICAL CONGENITAL ADRENAL HYPERPLASIA Anastasovska V1, Kocova E1, Kocova M1,2,* page: 19 UNUSUAL DETECTION OF TUBERCULOSIS IN A WOMAN WITH DOWN’S SYNDROME Pešut DP,1,2* Raljević S,2 Slijepčević Tomić Lj2,3 page: 61 Y CHROMOSOME SINGLE NUCLEOTIDE POLYMORPHISMS TYPING BY SNaPshot MINISEQUENCING Noveski P, Trivodalieva S, Efremov GD, Plaseska-Karanfilska D page: 11 TWO INFANTS WITH BECKWITH-WIEDEMANN SYNDROME Ratbi I1,2,*, Elalaoui SC1, Sefiani A1,2 page: 51

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