A carregar...

X inactivation of the FMR1 fragile X mental retardation gene.

X chromosome inactivation has been hypothesised to play a role in the aetiology and clinical expression of the fragile X syndrome. The identification of the FMR1 gene involved in fragile X syndrome allows testing of the assumption that the fragile X locus is normally subject to X inactivation. We st...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Kirchgessner, C U, Warren, S T, Willard, H F
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051769/
https://ncbi.nlm.nih.gov/pubmed/8825916
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!