vol 24
Number VOL. 24(2), 2021
8/8/2022
Front cover page: The Virgin Mary, Epitrachelion (detail), embroidery with gold and silver thread on a silk foundation, Monastery Putna, 1496 year, Putna, Romania.

Back cover page: Epitrachelion (detail), embroidery with gold and silver thread on a silk foundation, Monastery Putna, 1496 year, Putna, Romania
Cover design: Bitrakova-Grozdanova V, Skopje
ASSOCIATION OF RELATIVE TELOMERE LENGTH AND RISK OF HIGH HUMAN PAPILLOMAVIRUS LOAD IN CERVICAL EPITHELIAL CELLS
Albosale A H, Mashkina E V
page: 65
48,XYYY: A RARE CASE REPORT
Sabnis AS, Bhusare D
page: 103
CASE REPORT FOR TWO SIBLINGS CARRYING NEUROFIBROMATOSIS TYPE 1 WITH A RARE NF1: c.5392C>T MUTATION
Sayın Kocakap DB, Gündüz Ö, Özer L, Durak M
page: 99
NOVEL GPC3 GENE MUTATION IN SIMPSON-GOLABIBEHMEL SYNDROME WITH ENDOCRINE ANOMALIES: A CASE REPORT
Bu W, Zhu M, Li S, Liu H, Liu X,
page: 95
DE NOVO TINF2 C.845G>A: PATHOGENIC VARIANT IN PATIENT WITH DYSKERATOSIS CONGENITA
Kocheva SA, Gjorgjievska M, Martinova K, Antevska-Trajkova Z, Jovanovska A, Plaseska-Karanfilska D
page: 89
PHENOTYPIC VARIABILITY OF 17Q12 MICRODELETION SYNDROME – THREE CASES AND REVIEW OF LITERATURE
Țuțulan-Cuniță A, Pavel AG, Dimos L, Nedelea M, Ursuleanu A, Neacșu AT, Budișteanu M, Stambouli D
page: 0
TARGETED microRNA PROFILING IN GASTRIC CANCER WITH CLINICAL ASSESSEMENT
Pehlevan Ozel H, Dinç T, Tiryaki RS2, Keşkus AG, Konu O, Kayilioglu SI, Coşkun F
page: 55
RISK FACTORS OF VENOUS THROMBOEMBOLISM IN SUDANESE PREGNANT WOMEN
Abdalhabib EK, Alfeel A, Ali EI, Ibrahim IK, Mobarki AA, Dobie G, Hamali HA, Saboor M,
page: 49
SINGLE-NUCLEOTIDE POLYMORPHISMS IN EXONIC AND PROMOTER REGIONS OF TRANSCRIPTION FACTORS OF SECOND HEART FIELD ASSOCIATED WITH SPORADIC CONGENITAL CARDIAC ANOMALIES
Wang E, Fan X, Nie Y, Zheng Z, Hu S,
page: 39
FREQUENCIES OF THE MEFV GENE MUTATIONS IN AZERBAIJAN
Huseynova LS1, Mammadova SN, Aliyeva KAA
page: 33
DETERMINATION OF CYSTIC FIBROSIS MUTATION FREQUENCY IN PRETERM AND TERM NEONATES WITH RESPIRATORY TRACT PROBLEMS
Tanriverdi S1, Polat M, Onay H
page: 25
ARRAY-BASED COMPARATIVE GENOMIC HYBRIDIZATION ANALYSIS IN CHILDREN WITH DEVELOPMENTAL DELAY/INTELLECTUAL DISABILITY
Türkyılmaz A, Geckinli BB, Tekin E, Ates EA, Yarali O, Cebi AH, Arman A
page: 15
CLINICAL EXPERIENCE OF NEUROLOGICAL MITOCHONDRIAL DISEASES IN CHILDREN AND ADULTS: A SINGLE-CENTER STUDY
Rogac M, Neubauer D, Leonardis L, Pecaric N, Meznaric M, Maver A, Sperl W, Garavaglia BM, Lamantea E, Peterlin B
page: 5
HAVING MULTIPLE RENAL CYSTS IN A YOUNG ADULT IS NOT ALWAYS A SIGN OF POLYCYSTIC KIDNEY DISEASE
Kaynar K, Kayıpmaz S, Çebi AH, Hüseynova S
page: 83



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The 9th Balkan Congress of Medical Genetics
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