KARAGÜZEL, G. Et Al. 2016. An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.. 55th annual ESPE (European Society for Paediatric Endocrinology) Meeting , (Paris, France), 1.

KARAGÜZEL, G., Mutlu, M., Çebi, A. H., Şahin, S., & Polat, R., (2016). An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome. . 55th annual ESPE (European Society for Paediatric Endocrinology) Meeting (pp.1). Paris, France

KARAGÜZEL, GÜLAY Et Al. "An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.," 55th annual ESPE (European Society for Paediatric Endocrinology) Meeting, Paris, France, 2016

KARAGÜZEL, GÜLAY Et Al. "An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.." 55th annual ESPE (European Society for Paediatric Endocrinology) Meeting , Paris, France, pp.1, 2016

KARAGÜZEL, G. Et Al. (2016) . "An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.." 55th annual ESPE (European Society for Paediatric Endocrinology) Meeting , Paris, France, p.1.

@conferencepaper{conferencepaper, author={GÜLAY KARAGÜZEL Et Al. }, title={An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.}, congress name={55th annual ESPE (European Society for Paediatric Endocrinology) Meeting}, city={Paris}, country={France}, year={2016}, pages={1} }