Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation / 中华妇产科杂志
Chinese Journal of Obstetrics and Gynecology
;
(12)2000.
Artigo
em Chinês
| WPRIM
| ID: wpr-574106
ABSTRACT
G mutation of SLC26A4, the parents and the second child were carriers of the same mutation, while the fetus had a wild-type form. Conclusion It is feasible to identify deafness related genes by screening for GJB2 and SLC26A4 mutation, thus providing correct prenatal diagnosis and avoiding deaf delivery of baby.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo diagnóstico
Idioma:
Chinês
Revista:
Chinese Journal of Obstetrics and Gynecology
Ano de publicação:
2000
Tipo de documento:
Artigo
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