«An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity». J. Clin. Endocrinol. Metab., 87, 6, 6-2002, pàg. 2623–8. DOI: 10.1210/jc.87.6.2623. PMID: 12050225.
«An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity». J. Clin. Endocrinol. Metab., 87, 6, 6-2002, pàg. 2623–8. DOI: 10.1210/jc.87.6.2623. PMID: 12050225.