Sadeghi, F. Et Al. 2008. Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.8 , 781-787.

Sadeghi, F., KUTLAY, N., BERBEROĞLU, M., Cetinkaya, E., AYCAN, Z., Kara, C., ... ILGIN RUHİ, H.(2008). Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.8, 781-787.

Sadeghi, F. Et Al. "Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.8, 781-787, 2008

Sadeghi, F. Et Al. "Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.8, pp.781-787, 2008

Sadeghi, F. Et Al. (2008) . "Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.8, pp.781-787.

@article{article, author={F. Sadeghi Et Al. }, title={Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2008, pages={781-787} }