14 Articles
Original Article
Accès libre | 29 déc. 2017
Detection of allelic variants of the POLE and POLD1 genes in colorectal cancer patients
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Accès libre | 29 déc. 2017
Differential expression of FGFRs signaling pathway components in bladder cancer: A step toward personalized medicine
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Accès libre | 29 déc. 2017
Superoxide dismutase 1 and 2 gene polymorphism in Turkish vitiligo patients
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Accès libre | 29 déc. 2017
Association of the MMP7 –181A>G promoter polymorphism with early onset of chronic obstructive pulmonary disease
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Accès libre | 29 déc. 2017
Increased frequency of MEFV genes in patients with epigastric pain syndrome
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Accès libre | 29 déc. 2017
The mitochondrial COI/tRNASER(UCN) G7444A mutation may be associated with hearing impairment in a Han Chinese family
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Accès libre | 29 déc. 2017
Polymorphism of the ADRB2 rs1042713 gene is not associated with spontaneous preterm birth: Analyses in a Slovenian sample and meta analysis
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Accès libre | 29 déc. 2017
Association between Osteoprotegerin gene polymorphisms and risk of coronary artery disease: A systematic review and meta-analysis
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Accès libre | 29 déc. 2017
Molecular characterization of iranian patients with inherited coagulation factor VII deficiency
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Accès libre | 29 déc. 2017
Association between inherited thrombophilia in pregnancy and micronucleus frequency in peripheral blood lymphocytes
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Accès libre | 29 déc. 2017
Association of placenta previa with a history of previous Cesarian deliveries and indications for a possible role of a genetic component
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Letter to the Editor
Accès libre | 29 déc. 2017
Female and male carriers of TAZ mutations need to be thoroughly investigated
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Accès libre | 29 déc. 2017
Epidermal growth factor receptor Mutation status: Does younger mean more frequently mutated?
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Case Report
Accès libre | 29 déc. 2017
Galactosialidosis in a newborn with a novel mutation in the CTSA gene presenting with transient hyperparathyroidism
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