Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations-Reference-Cited by-同舟云学术

Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations

Published:2010-07 Issue:2 Volume:94 Page:472-476
ISSN:0015-0282
Container-title:Fertility and Sterility
language:en
Short-container-title:Fertility and Sterility

Author:

Philibert Pascal,Audran Françoise,Pienkowski Catherine,Morange Isabelle,Kohler Birgit,Flori Elisabeth,Heinrich Claudine,Dacou-Voutetakis Catherine,Joseph Marie-Geneviève,Guedj Anne-Marie,Journel Hubert,Hecart-Bruna Annie-Claude,Khotchali Ines,Ten Svetlana,Bouchard Philippe,Paris Françoise,Sultan Charles

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference24 articles.

1. Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene;Melo;J Clin Endocrinol Metab,2003

2. Disorders linked to insufficient androgen action in male children;Sultan;Hum Reprod Update,2001

3. Sexual function in women with complete androgen insensitivity syndrome;Minto;Fertil Steril,2003

4. Molecular basis of androgen insensitivity;Brinkmann;Mol Cell Endocrinol,2001

5. Androgen receptor mutations and androgen insensitivity;McPhaul;Mol Cell Endocrinol,2002

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