| Literature DB >> 2563196 |
C J Brown1, S J Goss, D B Lubahn, D R Joseph, E M Wilson, F S French, H F Willard.
Abstract
The gene for the androgen receptor, mutations at which cause the X-linked androgen insensitivity syndrome, has been localized to the q11----q12 region of the human X chromosome by analysis, using a cloned cDNA for the androgen receptor, of somatic cell hybrid panels segregating portions of the X chromosome. A moderate-frequency HindIII RFLP has been found which should be useful in genetic linkage analysis of the various inherited forms of androgen insensitivity.Entities:
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Year: 1989 PMID: 2563196 PMCID: PMC1715398
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025