Wilms's tumour and aniridia: clinical and cytogenetic features.

A survey carried out to detect children with aniridia/Wilms's tumour syndrome identified 8 living and 3 dead children. The incidence of aniridia was found to be 1 in 43 among Wilms's tumour patients in the UK. The clinical features included complete bilaterial aniridia, cataracts, glaucoma...

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Detaylı Bibliyografya
Asıl Yazarlar: Shannon, R S, Mann, J R, Harper, E, Harnden, D G, Morten, J E, Herbert, A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1982
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1627794/
https://ncbi.nlm.nih.gov/pubmed/6289758
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