APA

Bakker B., Bikker H., Vulsma T., de Randamie J. S., Wiedijk B. M. & De Vijlder J. J. (20001115). Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update). : The Journal of clinical endocrinology and metabolism.

Chicago

Bakker B, Bikker H, Vulsma T, de Randamie J S, Wiedijk B M and De Vijlder J J. 20001115. Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update). : The Journal of clinical endocrinology and metabolism.

Harvard

Bakker B., Bikker H., Vulsma T., de Randamie J. S., Wiedijk B. M. and De Vijlder J. J. (20001115). Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update). : The Journal of clinical endocrinology and metabolism.

MLA

Bakker B, Bikker H, Vulsma T, de Randamie J S, Wiedijk B M and De Vijlder J J. Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update). : The Journal of clinical endocrinology and metabolism. 20001115.