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Molecular genetic analysis of chromosome 11p in familial Wilms tumour.

In the family reported here, a mother and both of her children developed a Wilms tumour, and all three tumours were of the relatively rare monomorphous epithelial histopathological subtype. Using restriction fragment length polymorphism analysis, both sibs were shown to inherit the same maternal all...

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Detaylı Bibliyografya
Asıl Yazarlar: Baird, P. N., Pritchard, J., Cowell, J. K.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 1994
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1969446/
https://ncbi.nlm.nih.gov/pubmed/7911030
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