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Page 1
Mutational analysis of Turkish galactosaemia patients.
Coskun T, Erkul E, Seyrantepe V, Ozgüç M, Tokatli A, Ozalp I. Coskun T, et al. Among authors: ozguc m. J Inherit Metab Dis. 1995;18(3):368-9. doi: 10.1007/BF00710438. J Inherit Metab Dis. 1995. PMID: 7474913 Clinical Trial. No abstract available.
Study of 12 mutations in Turkish cystic fibrosis patients.
Yilmaz E, Erdem H, Ozgüç M, Coşkun T, Ozçelik U, Göçmen A, Ozalp I. Yilmaz E, et al. Among authors: ozguc m. Hum Hered. 1995 May-Jun;45(3):175-7. doi: 10.1159/000154281. Hum Hered. 1995. PMID: 7542223
Mutation analysis in Turkish phenylketonuria patients.
Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. J Med Genet. 1993 Feb;30(2):129-30. doi: 10.1136/jmg.30.2.129. J Med Genet. 1993. PMID: 8445616 Free PMC article.
Molecular basis of mild hyperphenylalaninaemia in Turkey.
Yilmaz E, Cali F, Roman V, Ozalp I, Coşkun T, Tokatli A, Kalkanoğlu HS, Ozgüç M. Yilmaz E, et al. Among authors: ozguc m. J Inherit Metab Dis. 2000 Jul;23(5):523-5. doi: 10.1023/a:1005628717813. J Inherit Metab Dis. 2000. PMID: 10947211 No abstract available.
69 results