Loss of heterozygosity at 7p in Wilms' tumour development

Chromosome 7p alterations have been implicated in the development of Wilms' tumour (WT) by previous studies of tumour cytogenetics, and by our analysis of a constitutional translocation (t(1;7)(q42;p15)) in a child with WT and radial aplasia. We therefore used polymorphic microsatellite markers...

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Detalles Bibliográficos
Autores principales: Powlesland, R M, Charles, A K, Malik, K T A, Reynolds, P A, Pires, S, Boavida, M, Brown, K W
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363297/
https://www.ncbi.nlm.nih.gov/pubmed/10646884
http://dx.doi.org/10.1054/bjoc.1999.0922

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363297/
https://www.ncbi.nlm.nih.gov/pubmed/10646884
http://dx.doi.org/10.1054/bjoc.1999.0922

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