BİDECİ, A. Et Al. 2017. familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del. 10. international meeting of pediatric endocrinology , (Washington, Kiribati).

BİDECİ, A., DÖĞER, E., DEMET AKBAŞ, E., KILINÇ UĞURLU, A., GÜRAN, T., ÇAMURDAN, M. O., ... CİNAZ, P.(2017). familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del . 10. international meeting of pediatric endocrinology, Washington, Kiribati

BİDECİ, AYSUN Et Al. "familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del," 10. international meeting of pediatric endocrinology, Washington, Kiribati, 2017

BİDECİ, AYSUN Et Al. "familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del." 10. international meeting of pediatric endocrinology , Washington, Kiribati, 2017

BİDECİ, A. Et Al. (2017) . "familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del." 10. international meeting of pediatric endocrinology , Washington, Kiribati.

@conferencepaper{conferencepaper, author={AYSUN BİDECİ Et Al. }, title={familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del}, congress name={10. international meeting of pediatric endocrinology}, city={Washington}, country={Kiribati}, year={2017}}