APA

Ferrara A. M., De Sanctis L., Rossi G., Capuano S., Del Prete G., Zampella E., Gianino P., Corrias A., Fenzi G., Zannini M. & Macchia P. E. (20090902). Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis. : Journal of endocrinological investigation.

Chicago

Ferrara A M, De Sanctis L, Rossi G, Capuano S, Del Prete G, Zampella E, Gianino P, Corrias A, Fenzi G, Zannini M and Macchia P E. 20090902. Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis. : Journal of endocrinological investigation.

Harvard

Ferrara A. M., De Sanctis L., Rossi G., Capuano S., Del Prete G., Zampella E., Gianino P., Corrias A., Fenzi G., Zannini M. and Macchia P. E. (20090902). Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis. : Journal of endocrinological investigation.

MLA

Ferrara A M, De Sanctis L, Rossi G, Capuano S, Del Prete G, Zampella E, Gianino P, Corrias A, Fenzi G, Zannini M and Macchia P E. Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis. : Journal of endocrinological investigation. 20090902.