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Journal of Inherited Metabolic Disease|January 5, 2002
Mutation analysis in Turkish patients with hereditary fructose intoleranceA Dursun, H S Kalkanoğlu, T Coşkun, et al.Journal of Inherited Metabolic Disease|July 18, 2002
Maple syrup urine disease: mutation analysis in Turkish patientsA Dursun, M Henneke, K Ozgül, et al.Human Genetics|January 12, 2001
Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)A Romstad, H S Kalkanoğlu, T Coşkun, et al.European Journal of Pediatrics|December 1, 1990
Scleroderma-like skin lesions in two patients with phenylketonuriaT Coşkun, I Ozalp, G Kale, et al.The Turkish Journal of Pediatrics|October 1, 1990
Intracranial calcification in dihydropteridine reductase deficiencyT Coşkun, A Besim, I Ozalp, et al.Acta Paediatrica Japonica : Overseas Edition|September 24, 1998
The effect of live measles vaccines on serum vitamin A levels in healthy childrenS S Yalçin, K Yurdakök, I Ozalp, et al.Journal of Medical Genetics|February 1, 1993
Mutation analysis in Turkish phenylketonuria patientsM Ozgüç, I Ozalp, T Coşkun, et al.The Turkish Journal of Pediatrics|January 1, 1993
Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patientsM Ozgüç, I Ozalp, T Coşkun, et al.The Turkish Journal of Pediatrics|January 1, 1992
Beta-ketothiolase deficiency. A case reportB Altintaş, T Teziç, T Coşkun, et al.Journal of Inherited Metabolic Disease|January 1, 1991
Type I hereditary tyrosinaemia: presentation of 11 casesT Coşkun, I Ozalp, N Koçak, et al.Pageof 11