V. N. Baş Et Al. , "Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.," Journal of pediatric endocrinology & metabolism : JPEM , vol.25, pp.1153-6, 2012
Baş, 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 : JPEM , vol.25 , 1153-6.
Baş, V. N., Cangul, H., Agladioglu, S., Kendall, M., Cetinkaya, S., Maher, E., ... Aycan, Z.(2012). Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.. Journal of pediatric endocrinology & metabolism : JPEM , vol.25, 1153-6.
Baş, VEYSEL Et Al. "Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.," Journal of pediatric endocrinology & metabolism : JPEM , vol.25, 1153-6, 2012
Baş, VEYSEL N. Et Al. "Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.." Journal of pediatric endocrinology & metabolism : JPEM , vol.25, pp.1153-6, 2012
Baş, 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 : JPEM , vol.25, pp.1153-6.
@article{article, author={VEYSEL NİJAT BAŞ Et Al. }, title={Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.}, journal={Journal of pediatric endocrinology & metabolism : JPEM}, year=2012, pages={1153-6} }