E. N. Gonc Et Al. , "Genetic IGF1R defects: new cases expand the spectrum of clinical features," JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.43, no.12, pp.1739-1748, 2020
Gonc, E. N. Et Al. 2020. Genetic IGF1R defects: new cases expand the spectrum of clinical features. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.43, no.12 , 1739-1748.
Gonc, E. N., Ozon, Z., Oguz, S., Kabacam, S., Taskiran, E., Kiper, P., ... Utine, G.(2020). Genetic IGF1R defects: new cases expand the spectrum of clinical features. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.43, no.12, 1739-1748.
Gonc, ELMAS Et Al. "Genetic IGF1R defects: new cases expand the spectrum of clinical features," JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.43, no.12, 1739-1748, 2020
Gonc, ELMAS N. Et Al. "Genetic IGF1R defects: new cases expand the spectrum of clinical features." JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.43, no.12, pp.1739-1748, 2020
Gonc, E. N. Et Al. (2020) . "Genetic IGF1R defects: new cases expand the spectrum of clinical features." JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.43, no.12, pp.1739-1748.
@article{article, author={ELMAS NAZLI GÖNÇ Et Al. }, title={Genetic IGF1R defects: new cases expand the spectrum of clinical features}, journal={JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION}, year=2020, pages={1739-1748} }