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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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Bibliografske podrobnosti
Main Authors: Scott, R H, Stiller, C A, Walker, L, Rahman, N
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 2006
Teme:
Online dostop: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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