Cangul, H. Et Al. 2014. An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.. Journal of pediatric endocrinology & metabolism : JPEM , vol.27 , 1021-5.

Cangul, H., SAĞLAM, H., Saglam, Y., EREN, E., Dogan, D., Kendall, M., ... Tarim, Ö. F.(2014). An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.. Journal of pediatric endocrinology & metabolism : JPEM , vol.27, 1021-5.

Cangul, Hakan Et Al. "An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.," Journal of pediatric endocrinology & metabolism : JPEM , vol.27, 1021-5, 2014

Cangul, Hakan Et Al. "An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.." Journal of pediatric endocrinology & metabolism : JPEM , vol.27, pp.1021-5, 2014

Cangul, H. Et Al. (2014) . "An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.." Journal of pediatric endocrinology & metabolism : JPEM , vol.27, pp.1021-5.

@article{article, author={Hakan Cangul Et Al. }, title={An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.}, journal={Journal of pediatric endocrinology & metabolism : JPEM}, year=2014, pages={1021-5} }