Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion

OBJECTIVE: The aim of this study was to determine if there is a significant difference in the risk of developing Wilms tumour between patients with submicroscopic and those with visible deletions of the WT1 tumour suppressor gene. METHODS: To determine which subjects had WT1 deletions, high‐resoluti...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: van Heyningen, Veronica, Hoovers, Jan M N, de Kraker, Jan, Crolla, John A
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Group 2007
Aiheet:
Letter to JMG
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2652818/
https://ncbi.nlm.nih.gov/pubmed/17630404
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.051318
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