MENGEN, E. Et Al. 2016. Complete idiopathic hypogonadotropic hypogonadism due to homozygous GNRH1 mutations in the mutational hot spots in the region encoding the decapeptide. Hormone Research in Paediatrics , vol.85, no.2 , 107-111.

MENGEN, E., TUNC, S., KOTAN, L. D., NALBANTOGLU, O., Demir, K., GÜRBÜZ, F., ... TURAN, İ.(2016). Complete idiopathic hypogonadotropic hypogonadism due to homozygous GNRH1 mutations in the mutational hot spots in the region encoding the decapeptide. Hormone Research in Paediatrics , vol.85, no.2, 107-111.

MENGEN, Eda Et Al. "Complete idiopathic hypogonadotropic hypogonadism due to homozygous GNRH1 mutations in the mutational hot spots in the region encoding the decapeptide," Hormone Research in Paediatrics , vol.85, no.2, 107-111, 2016

MENGEN, Eda Et Al. "Complete idiopathic hypogonadotropic hypogonadism due to homozygous GNRH1 mutations in the mutational hot spots in the region encoding the decapeptide." Hormone Research in Paediatrics , vol.85, no.2, pp.107-111, 2016

MENGEN, E. Et Al. (2016) . "Complete idiopathic hypogonadotropic hypogonadism due to homozygous GNRH1 mutations in the mutational hot spots in the region encoding the decapeptide." Hormone Research in Paediatrics , vol.85, no.2, pp.107-111.

@article{article, author={Eda MENGEN Et Al. }, title={Complete idiopathic hypogonadotropic hypogonadism due to homozygous GNRH1 mutations in the mutational hot spots in the region encoding the decapeptide}, journal={Hormone Research in Paediatrics}, year=2016, pages={107-111} }