A unique point mutation in the androgen receptor gene in a family with complete androgen insensitivity syndrome**Presented at the 38th Annual Meeting of the Society of Gynecologic Investigation, San Antonio, Texas, March 20 to 23, 1991.
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology,Reproductive Medicine
Reference19 articles.
1. 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;Brown;Proc Natl Acad Sci USA,1988
2. Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism;Brown;Am J Hum Genet,1989
3. Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse;Migeon;Proc Natl Acad Sci USA,1981
4. Molecular cloning of human and rat complementary DNA encoding the androgen receptors;Chang;Science,1988
5. Cloning, structure and expression of a cDNA encoding the human androgen receptor;Trapman;Biochem Biophys Res Commun,1988
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3. Lexikon der Syndrome und Fehlbildungen;Lexikon der Syndrome und Fehlbildungen;1999
4. Molecular Biology and Function of the Androgen Receptor in Genital Development;Journal of Urology;1997-04
5. Molecular Biology and Function of the Androgen Receptor in Genital Development;The Journal of Urology;1997-04
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