Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome associated with a characteristic pattern of visceromegaly and predisposition to childhood tumours. BWS is a genetically heterogeneous disorder; most cases are sporadic but approximately 15% are familial and a small number of BWS p...

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Detalhes bibliográficos
Main Authors: Catchpoole, D, Lam, W W, Valler, D, Temple, I K, Joyce, J A, Reik, W, Schofield, P N, Maher, E R
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050940/
https://ncbi.nlm.nih.gov/pubmed/9152830
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