APA

Pearce S. H., Cheetham T., Imrie H., Vaidya B., Barnes N. D., Bilous R. W., Carr D., Meeran K., Shaw N. J., Smith C. S., Toft A. D., Williams G. & Kendall-Taylor P. (19990201). A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1. : American journal of human genetics.

Chicago

Pearce S H, Cheetham T, Imrie H, Vaidya B, Barnes N D, Bilous R W, Carr D, Meeran K, Shaw N J, Smith C S, Toft A D, Williams G and Kendall-Taylor P. 19990201. A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1. : American journal of human genetics.

Harvard

Pearce S. H., Cheetham T., Imrie H., Vaidya B., Barnes N. D., Bilous R. W., Carr D., Meeran K., Shaw N. J., Smith C. S., Toft A. D., Williams G. and Kendall-Taylor P. (19990201). A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1. : American journal of human genetics.

MLA

Pearce S H, Cheetham T, Imrie H, Vaidya B, Barnes N D, Bilous R W, Carr D, Meeran K, Shaw N J, Smith C S, Toft A D, Williams G and Kendall-Taylor P. A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1. : American journal of human genetics. 19990201.