APA

Cangul H., Schoenmakers N. A., Saglam H., Doganlar D., Saglam Y., Eren E., Kendall M., Tarim O., Barrett T. G., Chatterjee K. & Maher E. R. (20150302). A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism. : Journal of pediatric endocrinology & metabolism : JPEM.

Chicago

Cangul Hakan, Schoenmakers Nadia A, Saglam Halil, Doganlar Durmus, Saglam Yaman, Eren Erdal, Kendall Michaela, Tarim Omer, Barrett Timothy G, Chatterjee Krish and Maher Eamonn R. 20150302. A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism. : Journal of pediatric endocrinology & metabolism : JPEM.

Harvard

Cangul H., Schoenmakers N. A., Saglam H., Doganlar D., Saglam Y., Eren E., Kendall M., Tarim O., Barrett T. G., Chatterjee K. and Maher E. R. (20150302). A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism. : Journal of pediatric endocrinology & metabolism : JPEM.

MLA

Cangul Hakan, Schoenmakers Nadia A, Saglam Halil, Doganlar Durmus, Saglam Yaman, Eren Erdal, Kendall Michaela, Tarim Omer, Barrett Timothy G, Chatterjee Krish and Maher Eamonn R. A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism. : Journal of pediatric endocrinology & metabolism : JPEM. 20150302.