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.
Pomahacova, Renata
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
Publication Type: Case Reports; Journal Article
1804-7521
10.5507/bp.2018.067 doi
Androgen-Insensitivity Syndrome--diagnosis
Disorders of Sex Development--diagnosis
Female
Fetal Development--genetics
Gene Transfer, Horizontal
Genetic Predisposition to Disease
Humans
Male
Mutation
Receptors, Androgen--genetics
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
Publication Type: Case Reports; Journal Article
1804-7521
10.5507/bp.2018.067 doi
Androgen-Insensitivity Syndrome--diagnosis
Disorders of Sex Development--diagnosis
Female
Fetal Development--genetics
Gene Transfer, Horizontal
Genetic Predisposition to Disease
Humans
Male
Mutation
Receptors, Androgen--genetics