Aycan, Z., Savaş-Erdeve, Ş., Çetinkaya, S., Kurnaz, E., Keskin, M., Muratoğlu Şahin, N., . . . Ceylaner, G. (2018). Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty. J Clin Res Pediatr Endocrinol.

Aycan, Zehra, Şenay Savaş-Erdeve, Semra Çetinkaya, Erdal Kurnaz, Melikşah Keskin, Nursel Muratoğlu Şahin, Elvan Bayramoğlu, and Gülay Ceylaner. "Investigation of MKRN3 Mutation in Patients With Familial Central Precocious Puberty." J Clin Res Pediatr Endocrinol 2018.

Aycan, Zehra, et al. "Investigation of MKRN3 Mutation in Patients With Familial Central Precocious Puberty." J Clin Res Pediatr Endocrinol 2018.