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Results: 1-6 |
Results: 6

Authors: Kalkanoglu, HS Romstad, A Coskun, T Guttler, F
Citation: Hs. Kalkanoglu et al., Evaluation of a fetus at risk for dihydropteridine reductase deficiency bydirect mutation analysis using denaturing gradient gel electrophoresis, PRENAT DIAG, 21(10), 2001, pp. 868-870

Authors: Dursun, A Kalkanoglu, HS Coskun, T Tokatli, A Bittner, R Kocak, N Yuce, A Ozalp, I Boehme, HJ
Citation: A. Dursun et al., Mutation analysis in Turkish patients with hereditary fructose intolerance, J INH MET D, 24(5), 2001, pp. 523-526

Authors: Kalkanoglu, HS Coskun, T Aydogdu, SD Tokatli, A Gurgey, A
Citation: Hs. Kalkanoglu et al., Factor V Leiden mutation in Turkish patients with homozygous cystathioninebeta-synthase deficiency, J INH MET D, 24(3), 2001, pp. 367-369

Authors: Kalkanoglu, HS Anadol, D Yilmaz, E Coskun, T
Citation: Hs. Kalkanoglu et al., Phenylketonuria and cystic fibrosis in the same patient, PEDIATR INT, 42(1), 2000, pp. 92-93

Authors: Romstad, A Kalkanoglu, HS Coskun, T Demirkol, M Tokatli, A Dursun, A Baykal, T Ozalp, I Guldberg, P Guttler, F
Citation: A. Romstad et al., Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE), HUM GENET, 107(6), 2000, pp. 546-553

Authors: Yilmaz, E Cali, F Romano, V Ozalp, I Coskun, T Tokatli, A Kalkanoglu, HS Ozguc, M
Citation: E. Yilmaz et al., Molecular basis of mild hyperphenylalaninaemia in Turkey, J INH MET D, 23(5), 2000, pp. 523-524A
Risultati: 1-6 |