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European Journal of Ophthalmology|February 1, 2002
The phenotype of arg555trp mutation in a large Turkish family with corneal granular dystrophyH Kiratli, M Irkeç, K Ozgül, et al.Eye (London, England)|August 6, 2005
Exclusion of LCA5 locus in a consanguineous Turkish family with macular coloboma-type LCAR K Ozgül, B Bozkurt, H Kiratli, et al.Neuropediatrics|August 25, 2001
Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish familiesK Gücüyener, K Ozgül, C Paternotte, 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.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.Neuropediatrics|June 15, 2006
Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosumA Olmez, G Uyanik, R K Ozgül, et al.Clinical Genetics|September 14, 2007
Molecular analysis and long-term clinical evaluation of three siblings with Alström syndromeR K Ozgül, I Satman, G B Collin, et al.JIMD Reports|February 23, 2013
Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I diseaseA Dursun, R K Ozgül, S Sivri, et al.Pageof 1