Kırkgöz, T. Et Al. 2018. Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene. HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology , (Athens, Greece), 597.

Kırkgöz, T., Özhan, B., Çetin, G. O., Kaygusuz, S. B., Demircioğlu, S., Bereket, A., ... Güran, T.(2018). Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene . HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology (pp.597). Athens, Greece

Kırkgöz, TARIK Et Al. "Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene," HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, Athens, Greece, 2018

Kırkgöz, TARIK Et Al. "Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene." HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology , Athens, Greece, pp.597, 2018

Kırkgöz, T. Et Al. (2018) . "Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene." HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology , Athens, Greece, p.597.

@conferencepaper{conferencepaper, author={TARIK KIRKGÖZ Et Al. }, title={Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene}, congress name={HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology}, city={Athens}, country={Greece}, year={2018}, pages={597} }