Epigenetic Alterations of H19 and LIT1 Distinguish Patients with Beckwith-Wiedemann Syndrome with Cancer and Birth Defects

Beckwith-Wiedemann syndrome (BWS) is a congenital cancer-predisposition syndrome associated with embryonal cancers, macroglossia, macrosomia, ear pits or ear creases, and midline abdominal-wall defects. The most common constitutional abnormalities in BWS are epigenetic, involving abnormal methylatio...

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Detalhes bibliográficos
Publicado no:Am J Hum Genet
Main Authors: DeBaun, Michael R., Niemitz, Emily L., McNeil, D. Elizabeth, Brandenburg, Sheri A., Lee, Maxwell P., Feinberg, Andrew P.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2002
Assuntos:
Articles
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC384940/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11813134/
https://ncbi.nlm.nih.govhttps://doi.org/10.1086/338934
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