Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.


Baş V. N., Cangul H., Agladioglu S., Kendall M., Cetinkaya S., Maher E., ...More

Journal of pediatric endocrinology & metabolism : JPEM, vol.25, pp.1153-6, 2012 (SCI-Expanded) identifier identifier identifier