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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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Библиографические подробности
Главные авторы: Scott, R H, Stiller, C A, Walker, L, Rahman, N
Формат: Artigo
Язык:Inglês
Опубликовано: BMJ Group 2006
Предметы:
Online-ссылка: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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