7 results on '"Yesil, Gozde"'
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2. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population
3. Action myoclonus-renal failure syndrome: Electrophysiological analysis and clinical progression of two siblings
4. A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood
5. Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia
6. Congenital Agenesis of Scrotum and Labia Majora in Siblings
7. MRI and MRS findings in fucosidosis; a rare lysosomal storage disease
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