KOTAN, L. D. Et Al. 2021. Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism. GENETICS IN MEDICINE , vol.23, no.6 , 1008-1016.

KOTAN, L. D., Ternier, G., Cakir, A. D., EMEKSİZ, H. C., TURAN, İ., Delpouve, G., ... Kardelen, A. D.(2021). Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism. GENETICS IN MEDICINE , vol.23, no.6, 1008-1016.

KOTAN, LEMAN Et Al. "Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism," GENETICS IN MEDICINE , vol.23, no.6, 1008-1016, 2021

KOTAN, LEMAN D. Et Al. "Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism." GENETICS IN MEDICINE , vol.23, no.6, pp.1008-1016, 2021

KOTAN, L. D. Et Al. (2021) . "Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism." GENETICS IN MEDICINE , vol.23, no.6, pp.1008-1016.

@article{article, author={LEMAN DAMLA KOTAN Et Al. }, title={Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism}, journal={GENETICS IN MEDICINE}, year=2021, pages={1008-1016} }