Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines

Beckwith–Wiedemann Syndrome (BWS) is an overgrowth syndrome caused by a variety of molecular changes on chromosome 11p15.5. Children with BWS have a significant risk of developing Wilms tumours with the degree of risk being dependent on the underlying molecular mechanism. In particular, only a relat...

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Detalhes bibliográficos
Publicado no:Eur J Hum Genet
Main Authors: Brzezinski, Jack, Shuman, Cheryl, Choufani, Sanaa, Ray, Peter, Stavropoulos, Dmitiri J, Basran, Raveen, Steele, Leslie, Parkinson, Nicole, Grant, Ronald, Thorner, Paul, Lorenzo, Armando, Weksberg, Rosanna
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5558170/
https://ncbi.nlm.nih.gov/pubmed/28699632
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2017.102
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