İ. TURAN Et Al. , "Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome," HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.58, 2016
TURAN, İ. Et Al. 2016. Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome. HORMONE RESEARCH IN PAEDIATRICS , vol.86 , 58.
TURAN, İ., Hutchins, B. I., Hacihamdioglu, B., Ozbek, M. N., KOTAN, L. D., ÖZKAN, Y., ... Stoner, H.(2016). Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome. HORMONE RESEARCH IN PAEDIATRICS , vol.86, 58.
TURAN, İHSAN Et Al. "Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome," HORMONE RESEARCH IN PAEDIATRICS , vol.86, 58, 2016
TURAN, İHSAN Et Al. "Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.58, 2016
TURAN, İ. Et Al. (2016) . "Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome." HORMONE RESEARCH IN PAEDIATRICS , vol.86, p.58.
@article{article, author={İHSAN TURAN Et Al. }, title={Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2016, pages={58} }