Z. Aycan Et Al. , "Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism," Journal of Clinical Endocrinology and Metabolism , vol.102, no.9, pp.3085-3090, 2017
Aycan, Z. Et Al. 2017. Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism. Journal of Clinical Endocrinology and Metabolism , vol.102, no.9 , 3085-3090.
Aycan, Z., Cangul, H., Muzza, M., Bas, V. N., Fugazzola, L., Chatterjee, V. K., ... Persani, L.(2017). Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism. Journal of Clinical Endocrinology and Metabolism , vol.102, no.9, 3085-3090.
Aycan, Zehra Et Al. "Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism," Journal of Clinical Endocrinology and Metabolism , vol.102, no.9, 3085-3090, 2017
Aycan, Zehra Et Al. "Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism." Journal of Clinical Endocrinology and Metabolism , vol.102, no.9, pp.3085-3090, 2017
Aycan, Z. Et Al. (2017) . "Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism." Journal of Clinical Endocrinology and Metabolism , vol.102, no.9, pp.3085-3090.
@article{article, author={Zehra Aycan Et Al. }, title={Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism}, journal={Journal of Clinical Endocrinology and Metabolism}, year=2017, pages={3085-3090} }