Baris, I. Et Al. 2006. A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.91, no.10 , 4183-4187.

Baris, I., Arisoy, A. E., Smith, A., Agostini, M., Mitchell, C. S., Park, S. M., ... Halefoglu, A. M.(2006). A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.91, no.10, 4183-4187.

Baris, I. Et Al. "A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis," JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.91, no.10, 4183-4187, 2006

Baris, I. Et Al. "A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.91, no.10, pp.4183-4187, 2006

Baris, I. Et Al. (2006) . "A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.91, no.10, pp.4183-4187.

@article{article, author={I. Baris Et Al. }, title={A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis}, journal={JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM}, year=2006, pages={4183-4187} }