GÜRBÜZ, F. Et Al. 2018. A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency. european society of pediatric endocrinology 2018 , (Atina, Greece).

GÜRBÜZ, F., TURAN, İ., TAŞTAN, M., & YÜKSEL, B., (2018). A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency . european society of pediatric endocrinology 2018, Atina, Greece

GÜRBÜZ, FATİH Et Al. "A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency," european society of pediatric endocrinology 2018, Atina, Greece, 2018

GÜRBÜZ, FATİH Et Al. "A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency." european society of pediatric endocrinology 2018 , Atina, Greece, 2018

GÜRBÜZ, F. Et Al. (2018) . "A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency." european society of pediatric endocrinology 2018 , Atina, Greece.

@conferencepaper{conferencepaper, author={FATİH GÜRBÜZ Et Al. }, title={A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency}, congress name={european society of pediatric endocrinology 2018}, city={Atina}, country={Greece}, year={2018}}