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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]
