Potter Syndrome in a Fetus with Trisomy-8 mosaicism: Report of a Case
Korean Journal of Pathology
; : 336-342, 1986.
Article
en Ko
| WPRIM
| ID: wpr-42676
Biblioteca responsable:
WPRO
ABSTRACT
Since the identification of the C-group chromosome has been made possible by the introduction of banding technique, the features of the trisomy-8 syndrome have been defined. Most of them have been mosaics and have had similar clinical findings. A case of Trisomy-8 mosaicism confirmed by G-banding analysis by skin fibroblast and heart blood in a dead female fetus of 35 weeks of gestation is described.
Texto completo:
1
Índice:
WPRIM
Límite:
Female
/
Humans
Idioma:
Ko
Revista:
Korean Journal of Pathology
Año:
1986
Tipo del documento:
Article