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...

Full description

Bibliographic Details
Main Authors: MacCarthy, A, Bayne, A, Brownbill, P, Bunch, K, Diggens, N, Draper, G, Hawkins, M, Jenkinson, H, Kingston, J, Stiller, C, Vincent, T, Murphy, M
Format: Journal article
Language:English
Published: 2013

Similar Items