F. Özgüç Çömlek Et Al. , "Leydig cell hypoplasia type 1 diagnosed in early childhood with inactivating mutation in LHCGR gene," Oxford Medical Case Reports , vol.4, pp.153-155, 2021
Özgüç Çömlek, F. Et Al. 2021. Leydig cell hypoplasia type 1 diagnosed in early childhood with inactivating mutation in LHCGR gene. Oxford Medical Case Reports , vol.4 , 153-155.
Özgüç Çömlek, F., Yıldız, R., Seyrek, F., & Tütüncüler, F., (2021). Leydig cell hypoplasia type 1 diagnosed in early childhood with inactivating mutation in LHCGR gene. Oxford Medical Case Reports , vol.4, 153-155.
Özgüç Çömlek, Fatma Et Al. "Leydig cell hypoplasia type 1 diagnosed in early childhood with inactivating mutation in LHCGR gene," Oxford Medical Case Reports , vol.4, 153-155, 2021
Özgüç Çömlek, Fatma Ö. Et Al. "Leydig cell hypoplasia type 1 diagnosed in early childhood with inactivating mutation in LHCGR gene." Oxford Medical Case Reports , vol.4, pp.153-155, 2021
Özgüç Çömlek, F. Et Al. (2021) . "Leydig cell hypoplasia type 1 diagnosed in early childhood with inactivating mutation in LHCGR gene." Oxford Medical Case Reports , vol.4, pp.153-155.
@article{article, author={Fatma Özgüç Çömlek Et Al. }, title={Leydig cell hypoplasia type 1 diagnosed in early childhood with inactivating mutation in LHCGR gene}, journal={Oxford Medical Case Reports}, year=2021, pages={153-155} }