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Öğe Lack of genotype-phenotype correlation for Kindlin-1 mutations in Kindler syndrome and evidence for possible genetic heterogeneity(Wiley-Blackwell, 2008) Lai-Cheong, J.; Liu, L.; Taskesen, M.; Akdeniz, S.; Maari, C.; Emanuel, P.; McGrath, J. A.[Abstract Not Available]Öğe Netherton syndrome resulting from a novel homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree(Wiley-Blackwell, 2011) Lai-Cheong, J.; Fong, K.; Akdeniz, S.; Isi, H.; Taskesen, M.; McGrath, J. A.[Abstract Not Available]Öğe OXIDATIVE STRESS IN CHILDREN WITH CONGENITAL HEART DISEASE: MEASUREMENTS OF MALONDIALDEHYDE, PROTEIN CARBONYL AND TOTAL ANTIOXIDANT CAPACITY AND THEIR ASSOCIATION WITH ACUTE PHASE REACTANTS AND PROINFLAMMATORY CYTOKINES(Wiley-Blackwell Publishing, Inc, 2010) Pirinccioglu, A. G.; Aylan, O.; Kizil, G.; Taskesen, M.; Kangin, M.; Beyazit, N.; Gunel, M. E.[Abstract Not Available]Öğe A ZINC SULPHATE-RESISTANT ACRODERMATITIS ENTEROPATHICA PATIENT WITH A NOVEL MUTATION IN SLC39A4 GENE(Springer, 2011) Kilic, M.; Taskesen, M.; Coskun, T.; Gurakan, F.; Tokatli, A.; Kalkanoglu-Sivri, H. S.; Dursun, A.[Abstract Not Available]
