Učitavanje...
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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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BMJ Group
2006
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| Teme: | |
| Online pristup: | 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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