Ara
Toplam kayıt 3, listelenen: 1-3
Fatal Outcome After Renal Transplant in a Pediatric Patient With Noonan Syndrome
(2015)
Noonan syndrome is a congenital, common, hereditary disorder. Facial dysmorphism, growth retardation, and various heart defects are typical clinical features. In patients with minor cardiac pathology, life expectancy is ...
Association of rs10757274 and rs2383206 Polymorphisms on 9p21 locus with Coronary Artery Disease in Turkish Population
(2016)
Background and Objectives: Genetic predisposition is an important risk factor for coronary artery disease (CAD). In this study, we aimed to evaluate the impact of rs10757274 and rs2383206 polymorphisms in chromosome 9p21 ...
Investigation of SOSTDC1 gene in non-syndromic patients with supernumerary teeth
(2018)
Background: The etiology of supernumerary teeth is still unclear however heredity is believed to be a major factor and this idea was supported by several case reports. Recently, a relationship between supernumerary tooth ...