Molecular Biology of Human Androgen Insensitivity Syndrome
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4612-2638-3_27.pdf
Reference36 articles.
1. Brown TR, Migeon CJ. Androgen insensitivity syndromes: paradox of phenotypic feminization with male genotype and normal testicular androgen secretion. In: Cohen MP, Foa PP, eds. Hormone resistance and other endocrine paradoxes. New York: Springer-Verlag, 1987:157–203.
2. Lubahn DB, Joseph DR, Sar M, et al. The human androgen receptor: complementary deoxyribonucleic acid cloning, sequence analysis, and gene expression in prostate. Mol Endocrinol 1988;2:1265–75.
3. Chang C, Kokontis J, Liao S. Structural analysis of complementary DNA and amino acid sequences of human and rat androgen receptors. Proc Natl Acad Sci USA 1988;85:7211–5.
4. Migeon BR, Brown TR, Axelman J, Rothwell SW, Migeon CJ. Studies on the locus for androgen receptor localization on the human X-chromosome and evidence for homology with the Tfm locus in the mouse. Proc Natl Acad Sci USA 1981;78:6339–43.
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1. Human Androgen Insensitivity Syndrome;Journal of Andrology;1995-07-08
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