Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21
Paripović, A, Maver, A, Stajić, N, Putnik, J, Ostojić, S, Alimpić, B, Ilić, N, Sarajlija, A
Diagnosis of Fanconi's Anemia by Diepoxybutane Analysis in Children from Serbia
Cirkovic, S, Guc-Scekic, M, Vujic, D, Ilic, N, Micic, D, Skoric, D, Jovanovic, A
Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency
Parezanović, M, Ilić, N, Ostojić, S, Stevanović, G, Ječmenica, J, Maver, A, Sarajlija, A
Phenotypic Variability of Cowden Syndrome Within a Single Family: Impact on Diagnosis, Management and Genetic Counselling
Ilic, N, Mitrovic, N, Radeta, R, Krasić, S, Vukomanović, V, Samardzija, G, Vasic, M, Vlahovic, A, Sarajlija, A