S. Bolu Et Al. , "Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature," TURKISH JOURNAL OF PEDIATRICS , vol.62, no.5, pp.851-857, 2020
Bolu, S. Et Al. 2020. Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature. TURKISH JOURNAL OF PEDIATRICS , vol.62, no.5 , 851-857.
Bolu, S., Eroz, R., TEKİN, M., & Dogan, M., (2020). Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature. TURKISH JOURNAL OF PEDIATRICS , vol.62, no.5, 851-857.
Bolu, Semih Et Al. "Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature," TURKISH JOURNAL OF PEDIATRICS , vol.62, no.5, 851-857, 2020
Bolu, Semih Et Al. "Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature." TURKISH JOURNAL OF PEDIATRICS , vol.62, no.5, pp.851-857, 2020
Bolu, S. Et Al. (2020) . "Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature." TURKISH JOURNAL OF PEDIATRICS , vol.62, no.5, pp.851-857.
@article{article, author={Semih Bolu Et Al. }, title={Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature}, journal={TURKISH JOURNAL OF PEDIATRICS}, year=2020, pages={851-857} }