DEMİRBAŞ, M. H. Et Al. 2019. International Participated Erciyes Medical Genetics Days 2019A novel mutation in HECW2 gene resulting neurodevelopmental disorder with hypotonia, seizures, and absent language. Erciyes Medical Journal , 25.

DEMİRBAŞ, M. H., ÖZBUDAK, P., SERDAROĞLU, A., & PERÇİN, F. E., (2019). International Participated Erciyes Medical Genetics Days 2019A novel mutation in HECW2 gene resulting neurodevelopmental disorder with hypotonia, seizures, and absent language. Erciyes Medical Journal , 25.

DEMİRBAŞ, MUSTAFA Et Al. "International Participated Erciyes Medical Genetics Days 2019A novel mutation in HECW2 gene resulting neurodevelopmental disorder with hypotonia, seizures, and absent language," Erciyes Medical Journal , 25, 2019

DEMİRBAŞ, MUSTAFA H. Et Al. "International Participated Erciyes Medical Genetics Days 2019A novel mutation in HECW2 gene resulting neurodevelopmental disorder with hypotonia, seizures, and absent language." Erciyes Medical Journal , pp.25, 2019

DEMİRBAŞ, M. H. Et Al. (2019) . "International Participated Erciyes Medical Genetics Days 2019A novel mutation in HECW2 gene resulting neurodevelopmental disorder with hypotonia, seizures, and absent language." Erciyes Medical Journal , p.25.

@article{article, author={MUSTAFA HAKAN DEMİRBAŞ Et Al. }, title={International Participated Erciyes Medical Genetics Days 2019A novel mutation in HECW2 gene resulting neurodevelopmental disorder with hypotonia, seizures, and absent language}, journal={Erciyes Medical Journal}, year=2019, pages={25} }