İNCECİK, F. And Herguner, O. M. 2017. Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency. ACTA NEUROLOGICA BELGICA , vol.117, no.3 , 779-780.

İNCECİK, F., & Herguner, O. M., (2017). Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency. ACTA NEUROLOGICA BELGICA , vol.117, no.3, 779-780.

İNCECİK, FARUK, And Ozlem M. Herguner. "Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency," ACTA NEUROLOGICA BELGICA , vol.117, no.3, 779-780, 2017

İNCECİK, FARUK And Herguner, Ozlem M. . "Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency." ACTA NEUROLOGICA BELGICA , vol.117, no.3, pp.779-780, 2017

İNCECİK, F. And Herguner, O. M. (2017) . "Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency." ACTA NEUROLOGICA BELGICA , vol.117, no.3, pp.779-780.

@article{article, author={FARUK İNCECİK And author={Ozlem M. Herguner}, title={Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency}, journal={ACTA NEUROLOGICA BELGICA}, year=2017, pages={779-780} }