Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene*-Reference-Cited by-同舟云学术

Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene*

Published:2010-09-02 Issue:3 Volume:40 Page:297-302
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Lobaccaro Jean-Marc,Belon Charles,Lumbroso Serge,Olewniczack Georges,Carré-Pigeon Françoise,Job Jean-Claude,Chaussain Jean-Louis,Toublanc Jean-Edmond,Sultan† Charles

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.1994.tb03922.x/fullpdf

Reference40 articles.

1. Partial androgen insensitivity: the Reifenstein syndrome revised;Amrhein;New England Journal of Medicine,1977

2. Androgen insensitivity in men: evidence for genetic heterogeneity;Amrhein;Proceedings of the National Academy of Sciences.,1976

3. Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome;Batch;Human Molecular Genetics,1992

4. Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism;Brown;American Journal of Human Genetics,1989

5. Deletion of the steroid-binding domain of the human androgen receptor in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity of this syndrome;Brown;Proceedings of the National Academy of Sciences.,1988

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