Congenital Hypothyroidism, Cerebellar Atrophy, and the Incomplete Phenotypic Expression of PHACES Syndrome

Endocrine Journal

Elisa BIAMINO¹  Margherita SILENGO¹  Andrea CORRIAS²  Giuseppina BALDASSARRE¹  Alessandro MUSSA² 

[1] Clinical Genetics, Department of Paediatrics, University of Torino;Pediatric Endocrinology, Department of Paediatrics, University of Torino

关键词: Androgen insensitivity syndrome;    Androgen receptor;    Gene;    Mutation;    Gender identity;   

DOI  :  10.1507/endocrj.K07E-155

学科分类：内分泌与代谢学

来源: Japan Endocrine Society

【 授权许可】

Unknown