KARDELEN, A. D. Et Al. 2017. A rare cause of congenital adrenal hyperplasia: Clinical and genetic findings and follow-up of six patients with 17 hydroxylase deficiency.. 10 th International Meeting of Pediatric Endocrinology , (Washington, Kiribati), 457-458.

KARDELEN, A. D., BAŞ, F., TOKSOY, G., POYRAZOĞLU, Ş., BUNDAK, R., ALTUNOĞLU, U., ... NAJAFLI, A.(2017). A rare cause of congenital adrenal hyperplasia: Clinical and genetic findings and follow-up of six patients with 17 hydroxylase deficiency. . 10 th International Meeting of Pediatric Endocrinology (pp.457-458). Washington, Kiribati

KARDELEN, ASLI Et Al. "A rare cause of congenital adrenal hyperplasia: Clinical and genetic findings and follow-up of six patients with 17 hydroxylase deficiency.," 10 th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 2017

KARDELEN, ASLI D. Et Al. "A rare cause of congenital adrenal hyperplasia: Clinical and genetic findings and follow-up of six patients with 17 hydroxylase deficiency.." 10 th International Meeting of Pediatric Endocrinology , Washington, Kiribati, pp.457-458, 2017

KARDELEN, A. D. Et Al. (2017) . "A rare cause of congenital adrenal hyperplasia: Clinical and genetic findings and follow-up of six patients with 17 hydroxylase deficiency.." 10 th International Meeting of Pediatric Endocrinology , Washington, Kiribati, pp.457-458.

@conferencepaper{conferencepaper, author={ASLI DERYA KARDELEN Et Al. }, title={A rare cause of congenital adrenal hyperplasia: Clinical and genetic findings and follow-up of six patients with 17 hydroxylase deficiency.}, congress name={10 th International Meeting of Pediatric Endocrinology}, city={Washington}, country={Kiribati}, year={2017}, pages={457-458} }