vol 23
Number VOL. 23, 2020 Acepted articles
8/10/2020
Front cover page: 0

Back cover page: 0
Cover design: 0
THE INTERACTION OF FEMALE AGE AND ACTIVE MALE SMOKING HAS NEGATIVE INFLUENCE ON SUCCESS RATES OF THE IN VITRO FERTILIZATION TREATMENTS
Petanovska Kostova E*
page: 1
THE EFFECTS OF O6-METHYL GUANINE DNA-METHYL TRANSFERASE PROMOTOR METHYLATION AND CpG1, CpG2, CpG3 AND CpG4 METHYLATION ON TREATMENT RESPONSE AND THEIR PROGNOSTIC SIGNIFICANCE IN PATIENTS WITH GLIOBLASTOMA
Yildiz OG1,*, Aslan D1, Akalin H2, Erdem Y3, Canoz O4, Aytekin A5, Ozoner S1, Dundar M2
page: 1
RELATIONSHIP BETWEEN CHROMOSOMAL ABERRATIONS AND GENE EXPRESSIONS IN THE p53 PATHWAY IN CHRONIC LYMPHOCYTIC LEUKEMIA
Öztan G1,*, Aktan M2, Palanduz S1, İşsever H3, Öztürk S1, Nikerel E4, Uçur A1, Bağatir G1, Bayrak A1, Çefle K1
page: 1
IMPLICATION OF VDR rs7975232 AND FCGR2A rs1801274 GENE POLYMORPHISMS IN THE RISK AND THE PROGNOSIS OF AUTOIMMUNE THYROID DISEASES IN THE TUNISIAN POPULATION
Mestiri S1,*, Zaaber I1, Nasr I1, Marmouch H2
page: 1
EVALUATION OF MicroRNA-124 EXPRESSION IN RENAL CELL CARCINOMA
Çaykara B, Öztürk G, Alsaadoni H, Ötünçtemur A, Pençe S
page: 73
DE NOVO KMT2D HETEROZYGOUS FRAMESHIFT DELETION IN A NEWBORN WITH A CONGENITAL HEART ANOMALY
Stangler Herodež Š1,2, Marčun Varda N2,3, Kokalj Vokač N1,2, Krgović D1,2,*
page: 1
A VERY RARE PARTIAL TRISOMY SYNDROME: DE NOVO DUPLICATION OF 16q12.1q23.3 IN A TURKISH GIRL WITH DEVELOPMENTAL DELAY AND FACIAL DYSMORPHIC FEATURES
Türkyılmaz A*, Yaralı O
page: 1
EFFECT OF EXOGENOUS TRANSCRIPTION FACTORS INTEGRATION SITES ON SAFETY AND PLURIPOTENCY OF INDUCED PLURIPOTENT STEM CELLS
Yin S1,*, Li W2,3,*, Yang G2,3, Cheng Y2,3, Yi Q1, Fan S1,2,3, Ma Q2,3, Zeng F1,2,3,
page: 1
AN INVESTIGATION OF THE COMT GENE VAL158MET POLYMORPHISM IN PATIENTS ADMITTED TO THE EMERGENCY DEPARTMENT BECAUSE OF SYNTHETIC CANNABINOID USE
Nennicioglu Y1, Kaya H2,*, Eraybar S2, Atmaca S2, Gorukmez O3, Armagan E4
page: 1
β-ELEMENE INHIBITS THE PROLIFERATION AND MIGRATION OF HUMAN GLIOBLASTOMA CELL LINES VIA SUPPRESSING RING FINGER PROTEIN 135
Alizada M1, Li J1, Aslami H2, Yang D3, Korchuganova T4, Xu YH1,*
page: 1
A NEW SPLICE-SITE MUTATION OF SPINK5 GENE IN THE NETHERTON SYNFROME WITH DIFFERENT CLINICAL FEATURES: A CASE REPORT
Erden E1,*, Ceylan AC2, Emre S1
page: 1
ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP-PALATE SYNDROME DUE TO A NOVEL MISSENSE MUTATION IN THE SAM DOMAIN OF THE TP63 GENE
Tajir M1,2,3,*, Lyahyai J1,2, Guaoua S1,2, El Alloussi M4, Sefiani A1,2
page: 1
RANKL IS A NEW EPIGENETIC BIOMARKER FOR THE VASOMOTOR SYMPTOM DURING MENOPAUSE
Kalkan R1,2,*, Altarda M1, Tosun O3
page: 1
PRENATAL DIAGNOSIS OF A DE NOVO PARTIAL TRISOMY 6q AND PARTIAL MONOSOMY 18p ASSOCIATED WITH CEPHALOCELE: A CASE REPORT
Karaman A1,*, Karaman B2, Çetinkaya A1,3, Karaman S4, Demirci O5
page: 1
ASSOCIATION OF THE BRAIN-DERIVED NEUROTROPHIC FACTOR Val66Met POLYMORPHISM WITH BODY MASS INDEX, FASTING GLUCOSE LEVELS AND LIPID STATUS IN ADOLESCENTS
Vidović V1,*, Maksimović N2, Novaković I2, Damnjanović T2, Jekić B2, Vidović S1, Majkić Singh N3, Stamenković-Radak M4, Nikolić D5, Marisavljević D6
page: 1
THE EXPRESSION LEVELS OF microRNAs ASSOCIATED WITH T AND B CELL DIFFERENTIATION/STIMULATION IN ANKYLOSING SPONDYLITIS
Türkyilmaz A1,*, Ata P1, Akbaş F2, Yağci İ2
page: 1



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VOL. 24(2), 2021 Accepted articles
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VOL. 24(1), 2021
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VOL. 23(2), 2020
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The 9th Balkan Congress of Medical Genetics
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