Novel mutation of MAP3K1 gene in 46,XY DSD with complete gonadal dysgenesis
Objective: Swyer syndrome, or 46, XY complete gonadal dysgenesis, is a disorder of human sexual development which present with female external genitalia, lack of female reproductive organs, and a 46, XY karyotype. Many genes that participate in human sexual development have been implicated in the pa...
Guardat en:
| Autors principals: | , , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2022-09-01
|
| Col·lecció: | Taiwanese Journal of Obstetrics & Gynecology |
| Matèries: | |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S1028455922002297 |
| Etiquetes: |
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|