Cangul, H. Et Al. 2014. A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4 , 323-327.

Cangul, H., AYCAN, Z., Kendall, M., Bas, V. N., Saglam, Y., Barrett, T. G., ... Maher, E. R.(2014). A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, 323-327.

Cangul, Hakan Et Al. "A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, 323-327, 2014

Cangul, Hakan Et Al. "A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, pp.323-327, 2014

Cangul, H. Et Al. (2014) . "A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.3-4, pp.323-327.

@article{article, author={Hakan Cangul Et Al. }, title={A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2014, pages={323-327} }