Pomahacova, Renata <br/><br/>
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.  [electronic resource] 

 -  Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia  Dec 2019 
 - 379-382 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1804-7521 
<br/><br/><label>Standard No.: </label>10.5507/bp.2018.067  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Androgen-Insensitivity Syndrome--diagnosis<br/>Disorders of Sex Development--diagnosis<br/>Female<br/>Fetal Development--genetics<br/>Gene Transfer, Horizontal<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Mutation<br/>Receptors, Androgen--genetics