Baş, S. Et Al. 2016. Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect. JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.8 , 14.

Baş, S., GÜRAN, T., Atay, Z., HALİLOĞLU, B., ABALI, S., DEMİRCİOĞLU, S., ... BEREKET, A.(2016). Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect. JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.8, 14.

Baş, Serpil Et Al. "Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect," JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.8, 14, 2016

Baş, Serpil Et Al. "Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect." JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.8, pp.14, 2016

Baş, S. Et Al. (2016) . "Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect." JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.8, p.14.

@article{article, author={Serpil Baş Et Al. }, title={Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect}, journal={JCRPE Journal of Clinical Research in Pediatric Endocrinology}, year=2016, pages={14} }