
15 Artikel
Original Article
PCSK9 gene participates in the development of primary dyslipidemias
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Association of NFKB1 , NKX2-5 , GATA4 and RANKL gene polymorphisms with sporadic congenital heart disease in Greek patients
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Increased expression of Cardiotrophin-1 in cardiomyopathy patients
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Dual effect of the GHRL gene variant in the molecular pathogenesis of obesity
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Comparative analysis of genes associated with obesity in humans using bioinformatic data and tools
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Two years of newborn screening for cystic fibrosis in North Macedonia: First experience
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Genetic association of solute carrier transporter gene variants with metformin response
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Simultaneously both expression of LMP-1 and methylation of E-cadherin : Molecular biomarker in stage IV of nasopharyngeal carcinoma patients
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Mutation status and immunohistochemical correlation of EGFR mutations in gastrointestinal stromal tumors
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GA genotype of the Arg280His polymorphism on the XRCC1 gene: Genetic susceptibility genotype in differentiated thyroid carcinomas?
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Familial atypical hemolytic uremic syndrome with positive p.S1191L (c.3572C>T) mutation on the CFH gene: A single-center experience
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Duplication of chromosome 16p13.11-p12.3 with different expressions in the same family
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Case Report
Novel mutation in the COL11A1 gene causing Marshall-Stickler syndrome in three generations of a Bulgarian family
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Smith-Lemli-Opitz syndrome: Bosnian and Herzegovinian experience
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A case of glycogen storage disease type 1a mimicking familial chylomicronemia syndrome
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