Late diagnosis of complete androgen insensitivity syndrome and transmission/carriers of the condition in a family with mutation c.2495G> T p.(Arg832Leu) in exon 7 of the androgen receptor gene: genetic, clinical and ethical aspects-Reference-Cited by-同舟云学术

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Late diagnosis of complete androgen insensitivity syndrome and transmission/carriers of the condition in a family with mutation c.2495G> T p.(Arg832Leu) in exon 7 of the androgen receptor gene: genetic, clinical and ethical aspects

Published:2019-12-11 Issue:4 Volume:163 Page:379-382
ISSN:1213-8118
Container-title:Biomedical Papers
language:
Short-container-title:BIOMED PAP

Author:

Pomahacova Renata,Zamboryova Jana,Paterova Petra,Krepelova Anna,Subrt Ivan,Jaklova Radka,Vohradska Petra,Hrdonkova Eliska,Sykora Josef

Publisher

Palacky University Olomouc

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://biomed.papers.upol.cz/doi/10.5507/bp.2018.067.pdf

Reference22 articles.

1. Disorders of sex development;Achermann JC,2011

2. Androgen insensitivity syndrome: clinical features and molecular defects

3. The Use of MRI in the Pre-surgical Evaluation of Patients with Androgen Insensitivity Syndrome

4. Imaging characteristics of androgen insensitivity syndrome

5. Androgen insensitivity syndrome

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