Complete androgen insensitivity due to a splice-site mutation in the androgen receptor gene and genetic screening with single-stranded conformation polymorphism*

Author:

Yong Eu Leong,Chua Kim Lee,Yang Mary,Roy Ashim,Ratnam Shan

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference16 articles.

1. Genetic basis of endocrine disease: the spectrum of mutations in the androgen receptor gene that causes androgen resistance;McPhaul;J Clin Endocrinol Metab,1993

2. Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status;Quigley;J Clin Endocrinol Metab,1992

3. Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes;Kazemi-Esfarjani;Mol Endocrinol,1993

4. Androgen resistance—the clinical and molecular spectrum;Griffin;N Engl J Med,1992

5. Variable androgen receptor levels in infertile men;Morrow;J Clin Endocrinol Metab,1987

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