Bas, V. N. Et Al. 2014. A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4 , 383-387.

Bas, V. N., AYCAN, Z., Cangul, H., Kendall, M., Agladioglu, S. Y., Cetinkaya, S., ... Maher, E. R.(2014). A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, 383-387.

Bas, Veysel Et Al. "A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, 383-387, 2014

Bas, Veysel N. Et Al. "A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, pp.383-387, 2014

Bas, V. N. Et Al. (2014) . "A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, pp.383-387.

@article{article, author={Veysel Nijat Bas Et Al. }, title={A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2014, pages={383-387} }