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«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, juny 2002, pàg. 2623–8. DOI: 10.1210/jc.87.6.2623. PMID: 12050225.
«Androgen receptor defects: historical, clinical, and molecular perspectives». Endocr. Rev., 16, 3, juny 1995, pàg. 271–321. DOI: 10.1210/edrv-16-3-271. PMID: 7671849.
«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, juny 2002, pàg. 2623–8. DOI: 10.1210/jc.87.6.2623. PMID: 12050225.