A very rare partial trisomy syndrome: De novo duplication of 16q12.1q23.3 in a Turkish girl with developmental delay and facial dysmorphic features

by Türkyılmaz A, Yaralı O
Published 2020-08-01

A Novel splice-site mutation on the MLC1 gene leading to exon 9 skipping and megalencephalic leukoencephalopathy with subcortical cysts in a Turkish patient

by Türkyılmaz A, Ünver O, Ekinci G, Türkdoğan D
Published 2019-12-01

The expression levels of microRNAs associated with T and B cell differentiation/stimulation in ankylosing spondylitis

by Türkyilmaz A, Ata P, Akbaş F, Yağci İ
Published 2020-08-01