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Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour
Wilms tumour has been reported in association with over 50 different clinical conditions and several abnormal constitutional karyotypes. Conclusive evidence of an increased risk of Wilms tumour exists for only a minority of these conditions, including WT1 associated syndromes, familial Wilms tumour,...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMJ Group
2006
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2564568/ https://ncbi.nlm.nih.gov/pubmed/16690728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.041723 |
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