Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.

Beckwith-Wiedemann syndrome (BWS) is an autosomal dominant disorder of increased prenatal growth and predisposition to embryonal cancers such as Wilms tumor. BWS is thought to involve one or more imprinted genes, since some patients show paternal uniparental disomy, and others show balanced germ-lin...

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Détails bibliographiques
Auteurs principaux: Lee, M P, DeBaun, M, Randhawa, G, Reichard, B A, Elledge, S J, Feinberg, A P
Format: Artigo
Langue:Inglês
Publié: 1997
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715913/
https://ncbi.nlm.nih.gov/pubmed/9311734
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