Bas, V. N. Et Al. 2012. Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.25, no.11-12 , 1153-1156.

Bas, V. N., Cangul, H., Agladioglu, S. Y., Kendall, M., Cetinkaya, S., Maher, E. R., ... AYCAN, Z.(2012). Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.25, no.11-12, 1153-1156.

Bas, Veysel Et Al. "Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.25, no.11-12, 1153-1156, 2012

Bas, Veysel N. Et Al. "Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.25, no.11-12, pp.1153-1156, 2012

Bas, V. N. Et Al. (2012) . "Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.25, no.11-12, pp.1153-1156.

@article{article, author={Veysel Nijat Bas Et Al. }, title={Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2012, pages={1153-1156} }