Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism.

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 chr...

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Bibliografiska uppgifter
Huvudupphovsmän: Brown, C J, Goss, S J, Lubahn, D B, Joseph, D R, Wilson, E M, French, F S, Willard, H F
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1989
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715398/
https://ncbi.nlm.nih.gov/pubmed/2563196
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