Browsing by Author "Percin, FE"
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Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3
Malik, S; Percin, FE; Ahmad, W; Percin, S; Akarsu, NA; Koch, MC; Grzeschik, KH (WILEY-LISS, 2005)Previously we have described a novel and distinct form of non-syndromic osseous syndactyly segregating in an autosomal recessive pattern in a consanguineous Pakistani family. The limb findings include mesoaxial reduction ... -
No association of polymorphisms in the glutathione S-transferase genes with pre-eclampsia, eclampsia and HELLP syndrome in a Turkish population
Cetin, M; Pinarbasi, E; Percin, FE; Akgun, E; Percin, S; Pinarbasi, H; Gurlek, F; Cetin, A (BLACKWELL PUBLISHING ASIA, 2005)Aim: There is substantial evidence that genetic factors play a role in pre-eclampsia. The aim of this study was to determine whether genetic variability in the encoding of genes for glutathione S-transferase M1 (GSTM1) and ...