
10 Artikel
Individual Phenotype Trait Variability as Genetic Markers of Gender Susceptibility to Spina Bifida
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Polymorphisms of HPC2/ELAC2 and SRD5A2 (5α-Reductase Type II) Genes in Prostate Cancer
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Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population
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Interleukin-18 Promoter Gene Polymorphisms are not Associated with Myocardial Infarction in Type 2 Diabetes in Slovenia
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Pulmonary Thromboembolism Following Radio-Frequency Ablation of the Atrioventricular Node in a Patient Heterozygous for the Factor V Leiden and the Mthfr C677T Mutations
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Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
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Detection of the GJB2 Mutation in Iranian Children with Hearing Loss Treated with Cochlear Implantation
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RLIP76 Gene Variants are not Associated with Drug Response in Turkish Epilepsy Patients
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Aplasia Ras Homologous Member I Gene and Development of Glial Tumors
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Partial Trisomy 9p(p22→pter) from a Maternal Translocation 4q35 and 9p22
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