Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
Dennis B. Lubahn(University of Missouri), Frank S. French(University of North Carolina at Chapel Hill), Henry N. Higgs(Dartmouth College), Claude J. Migeon, J A Simental(University of North Carolina at Chapel Hill), Elizabeth M. Wilson(University of North Carolina at Chapel Hill), T. R. Brown(Johns Hopkins University)
Cited by 447
Related Papers
Endocrine-Disrupting Chemicals and Public Health Protection: A Statement of Principles from The Endocrine Society
|Endocrinology|2012|1.2k
International Union of Pharmacology. LXV. The Pharmacology and Classification of the Nuclear Receptor Superfamily: Glucocorticoid, Mineralocorticoid, Progesterone, and Androgen Receptors
|Pharmacological Reviews|2006|430
Androgen receptor gene mutations in human prostate cancer.
|Proceedings of the National Academy of Sciences|1992|420
Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome.
|Proceedings of the National Academy of Sciences|1988|209
Micropenis. I. Criteria, etiologies and classification.
|PubMed|1980|190