H. Cangul 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 , vol.27, pp.1021-1025, 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 , vol.27 , 1021-1025.
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 , vol.27, 1021-1025.
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 , vol.27, 1021-1025, 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 , vol.27, pp.1021-1025, 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 , vol.27, pp.1021-1025.
@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}, year=2014, pages={1021-1025} }