Cangul, H. Et Al. 2014. A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.11-12 , 1101-1105.

Cangul, H., Bas, V. N., Saglam, Y., Kendall, M., Barrett, T. G., Maher, E. R., ... AYCAN, Z.(2014). A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.11-12, 1101-1105.

Cangul, Hakan Et Al. "A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.11-12, 1101-1105, 2014

Cangul, Hakan Et Al. "A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.11-12, pp.1101-1105, 2014

Cangul, H. Et Al. (2014) . "A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.11-12, pp.1101-1105.

@article{article, author={Hakan Cangul Et Al. }, title={A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2014, pages={1101-1105} }