KARAGÜZEL, G. Et Al. 2016. An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome. HORMONE RESEARCH IN PAEDIATRICS , vol.86 , 140-141.

KARAGÜZEL, G., MUTLU, M., CEBI, A., ŞAHİN, S., & POLAT, R., (2016). An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome. HORMONE RESEARCH IN PAEDIATRICS , vol.86, 140-141.

KARAGÜZEL, GÜLAY Et Al. "An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome," HORMONE RESEARCH IN PAEDIATRICS , vol.86, 140-141, 2016

KARAGÜZEL, GÜLAY Et Al. "An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.140-141, 2016

KARAGÜZEL, G. Et Al. (2016) . "An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.140-141.

@article{article, author={GÜLAY KARAGÜZEL Et Al. }, title={An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2016, pages={140-141} }