SAVAS-ERDEVE, S. Et Al. 2017. Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.7 , 759-766.

SAVAS-ERDEVE, S., CETINKAYA, S., Abali, Z. Y., Poyrazoglu, S., Bas, F., Berberoglu, M., ... Siklar, Z.(2017). Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.7, 759-766.

SAVAS-ERDEVE, Senay Et Al. "Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.7, 759-766, 2017

SAVAS-ERDEVE, Senay Et Al. "Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.7, pp.759-766, 2017

SAVAS-ERDEVE, S. Et Al. (2017) . "Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.7, pp.759-766.

@article{article, author={Senay SAVAS-ERDEVE Et Al. }, title={Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2017, pages={759-766} }