Detalhe da pesquisa
1.
Changes in the clinical management of 5α-reductase type 2 and 17ß-hydroxysteroid dehydrogenase type 3 deficiencies in France.
Endocr Connect
; 12(3)2023 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36606580
2.
Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?
Eur J Med Genet
; 63(4): 103812, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31731040
3.
Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder.
Front Endocrinol (Lausanne)
; 10: 625, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31572304
4.
Surgery in disorders of sex development (DSD) with a gender issue: If (why), when, and how?
J Pediatr Urol
; 12(3): 139-49, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27132944
5.
Surgical options in disorders of sex development (dsd) with ambiguous genitalia.
Best Pract Res Clin Endocrinol Metab
; 24(2): 311-24, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20541154