APA

Muzza M., Rabbiosi S., Vigone M. C., Zamproni I., Cirello V., Maffini M. A., Maruca K., Schoenmakers N., Beccaria L., Gallo F., Park S., Beck-Peccoz P., Persani L., Weber G. & Fugazzola L. (20140714). The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects. : The Journal of clinical endocrinology and metabolism.

Chicago

Muzza M, Rabbiosi S, Vigone M C, Zamproni I, Cirello V, Maffini M A, Maruca K, Schoenmakers N, Beccaria L, Gallo F, Park S-M, Beck-Peccoz P, Persani L, Weber G and Fugazzola L. 20140714. The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects. : The Journal of clinical endocrinology and metabolism.

Harvard

Muzza M., Rabbiosi S., Vigone M. C., Zamproni I., Cirello V., Maffini M. A., Maruca K., Schoenmakers N., Beccaria L., Gallo F., Park S., Beck-Peccoz P., Persani L., Weber G. and Fugazzola L. (20140714). The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects. : The Journal of clinical endocrinology and metabolism.

MLA

Muzza M, Rabbiosi S, Vigone M C, Zamproni I, Cirello V, Maffini M A, Maruca K, Schoenmakers N, Beccaria L, Gallo F, Park S-M, Beck-Peccoz P, Persani L, Weber G and Fugazzola L. The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects. : The Journal of clinical endocrinology and metabolism. 20140714.