A carregar...

Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome.

In an attempt to elucidate the role of methylation in parental imprinting at the IGF-II gene locus, for which imprinting has already been described in the mouse, we undertook an allele specific methylation study of the human IGF-II gene (mapped to 11p15.5) in a control population and in patients wit...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Schneid, H, Seurin, D, Vazquez, M P, Gourmelen, M, Cabrol, S, Le Bouc, Y
Formato: Artigo
Idioma:Inglês
Publicado em: 1993
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016368/
https://ncbi.nlm.nih.gov/pubmed/8320696
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!