Experience with the Ketogenic Diet in a Boy with CLCN4 Related Neurodevelopmental Disorder
Sager, G, Yukselmis, U, Güzel, O, Turkyilmaz, A, Akcay, M
Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability
Türkyılmaz, A, Geckinli, BB, Tekin, E, Ates, EA, Yarali, O, Cebi, AH, Arman, A
The expression levels of microRNAs associated with T and B cell differentiation/stimulation in ankylosing spondylitis
Türkyilmaz, A, Ata, P, Akbaş, F, Yağci, İ
A Novel splice-site mutation on the MLC1 gene leading to exon 9 skipping and megalencephalic leukoencephalopathy with subcortical cysts in a Turkish patient
Türkyılmaz, A, Ünver, O, Ekinci, G, Türkdoğan, D
A very rare partial trisomy syndrome: De novo duplication of 16q12.1q23.3 in a Turkish girl with developmental delay and facial dysmorphic features
Türkyılmaz, A, Yaralı, O
Novel KIF11 Variants with New Clinical Features: Expanding the Clinical Phenotype
Apuhan, T, Saglam Kubra, A, Yilmaz, M, Bebek, O, Demiroglu, S.A, Demir, O, Cebi, H.A, Turkyilmaz, A