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]

By: Contributor(s): Producer: 20200608Description: 379-382 p. digitalISSN:
  • 1804-7521
Subject(s): Online resources: In: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia vol. 163
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Publication Type: Case Reports; Journal Article

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