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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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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2000
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2363297/ https://ncbi.nlm.nih.gov/pubmed/10646884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1054/bjoc.1999.0922 |
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