İNCECİK, F. Et Al. 2017. Hydrocephalus is a rare clinical symptom in a child with multiple sulfatase deficiency. 12. EPNS Congress .

İNCECİK, F., HERGÜNER, M. Ö., & şeyda, b., (2017). Hydrocephalus is a rare clinical symptom in a child with multiple sulfatase deficiency . 12. EPNS Congress

İNCECİK, FARUK, M.ÖZLEM HERGÜNER, And beşen şeyda. "Hydrocephalus is a rare clinical symptom in a child with multiple sulfatase deficiency," 12. EPNS Congress, 2017

İNCECİK, FARUK Et Al. "Hydrocephalus is a rare clinical symptom in a child with multiple sulfatase deficiency." 12. EPNS Congress , 2017

İNCECİK, F. HERGÜNER, M. Ö. And şeyda, b. (2017) . "Hydrocephalus is a rare clinical symptom in a child with multiple sulfatase deficiency." 12. EPNS Congress .

@conferencepaper{conferencepaper, author={FARUK İNCECİK Et Al. }, title={Hydrocephalus is a rare clinical symptom in a child with multiple sulfatase deficiency}, congress name={12. EPNS Congress}, city={}, country={}, year={2017}}