Detalhe da pesquisa
1.
A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature Review.
Pediatr Endocrinol Rev
; 17(4): 302-307, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32780953