Konu "genotype" için Tıp Fakültesi Koleksiyonu listeleme
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Characterization of the apelin-1860T>C polymorphism in Turkish coronary artery disease patients and healthy individuals
(E-Century Publishing Corporation, 2015)To evaluate the association between the apelin -1860T>C polymorphism and plasma apelin levels in Turkish patients with coronary artery disease (CAD). A total of 276 individuals were enrolled in the present study, including ... -
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
(Nature Publishing Group, 2016)Purpose:Noonan syndrome (NS) is an autosomal-dominant disorder characterized by craniofacial dysmorphism, growth retardation, cardiac abnormalities, and learning difficulties. It belongs to the RASopathies, which are caused ...