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Clinical Genetics|May 1, 1994
Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis familiesM Ozgüç, E Yilmaz, H Erdem, et al.Pediatric Nephrology (Berlin, Germany)|October 1, 1996
A case of Pearson syndrome associated with multiple renal cystsA Gürgey, I Ozalp, A Rötig, et al.JIMD Reports|February 23, 2013
Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiencyM Kilic, R K Ozgül, T Coşkun, et al.Materia Medica Polona. Polish Journal of Medicine and Pharmacy|January 1, 1993
Leucocyte ascorbic acid concentration and plasma ascorbic acid levels in children with various infectionsF Tanzer, I OzalpInternational Journal of Pediatric Otorhinolaryngology|December 13, 2006
Audiologic findings in children with biotinidase deficiency in TurkeyG A Genc, H S Sivri-Kalkanoğlu, A Dursun, et al.The Journal of Pediatrics|March 20, 1998
Delayed-onset profound biotinidase deficiencyB Wolf, R J Pomponio, K J Norrgard, et al.Clinical Pediatrics|April 1, 1988
High levels of lactate, pyruvate, and alanine in anemic childrenM Ceyhan, I Ozalp, C AltayJournal of Inherited Metabolic Disease|January 1, 1991
Heterozygous carriers of classical phenylketonuria in a sample of the Turkish population: detection by a spectrofluorimetric methodF Güneral, I Ozalp, H TatlidilInternational Journal of Pediatric Otorhinolaryngology|May 1, 1992
Biotinidase deficiency: a rare cause of laryngeal stridorM Ataman, B Sözeri, I OzalpJournal of Tropical Pediatrics|October 1, 1990
Investigation of serum vitamin A levels of children who had a history of recurrent diarrhoea and acute respiratory infections in AnkaraB Büyükgebiz, I Ozalp, O OranPageof 11