AYCAN, Z. Et Al. 2017. Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.102, no.9 , 3085-3090.

AYCAN, Z., CANGÜL, 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 & 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 & 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 & 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 & 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 & METABOLISM}, year=2017, pages={3085-3090} }