Second and subsequent tumours among 1927 retinoblastoma patients diagnosed in Britain 1951–2004

BACKGROUND: Retinoblastoma is an eye tumour of childhood that occurs in heritable and non-heritable forms. In the heritable form, there is a predisposition to the development of non-ocular subsequent primary tumours (SPTs). METHODS: This study included 1927 retinoblastoma patients diagnosed in Brita...

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Autors principals: MacCarthy, A, Bayne, A M, Brownbill, P A, Bunch, K J, Diggens, N L, Draper, G J, Hawkins, M M, Jenkinson, H C, Kingston, J E, Stiller, C A, Vincent, T J, Murphy, M F G
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2013
Matèries:
Clinical Study
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3694232/
https://ncbi.nlm.nih.gov/pubmed/23674091
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/bjc.2013.228
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