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Balkan Journal of Medical Genetics : BJMG|January 17, 2020
Association of Genetic Polymorphisms in the Matrix Gla Protein (MGP) Gene with Coronary Artery Disease and Serum MGP LevelsS Karsli-Ceppioglu, S Yazar, Y Keskin, et al.Balkan Journal of Medical Genetics : BJMG|January 17, 2020
Clinical Next Generation Sequencing Reveals an H3F3A Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth RetardationA Maver, G Čuturilo, Stojanović J Ruml, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
Relationship between Chromosomal Aberrations and Gene Expressions in the p53 Pathway in Chronic Lymphocytic LeukemiaG Öztan, M Aktan, S Palanduz, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
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 GlioblastomaO G Yildiz, D Aslan, H Akalin, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
β-Elemene Inhibits the Proliferation and Migration of Human Glioblastoma Cell Lines via Suppressing Ring Finger Protein 135M Alizada, J Li, H Aslami, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
The Interaction of Female Age and Active Male Smoking has Negative Influence on Success Rates of the in Vitro Fertilization TreatmentsE Petanovska KostovaBalkan Journal of Medical Genetics : BJMG|September 21, 2020
Implication of VDR Rs7975232 and FCGR2A Rs1801274 Gene Polymorphisms in the Risk and the Prognosis of autoimmune Thyroid Diseases in the Tunisian PopulationS Mestiri, I Zaaber, I Nasr, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
Association of the Brain-derived Neurotrophic Factor Val66Met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in AdolescentsV Vidović, N Maksimović, I Novaković, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
De Novo KMT2D Heterozygous Frameshift Deletion in a Newborn with a Congenital Heart AnomalyŠ Stangler Herodež, N Marčun Varda, Kokalj Vokač N, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
A New Splice-site Mutation of SPINK5 Gene in the Netherton Syndrome with Different Clinical Features: A Case ReportE Erden, A C Ceylan, S EmrePageof 40