Cangul, H. Et Al. 2014. One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.3 , 169-173.

Cangul, H., Dogan, M., Saglam, Y., Kendall, M., Boelaert, K., Barrett, T. G., ... Maher, E. R.(2014). One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.3, 169-173.

Cangul, Hakan Et Al. "One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.3, 169-173, 2014

Cangul, Hakan Et Al. "One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.3, pp.169-173, 2014

Cangul, H. Et Al. (2014) . "One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.3, pp.169-173.

@article{article, author={Hakan Cangul Et Al. }, title={One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism}, journal={JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY}, year=2014, pages={169-173} }