Loss of heterozygosity at 7p in Wilms’ tumour development

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چکیده

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Loss of heterozygosity at 2q37 in sporadic Wilms' tumor: putative role for miR-562.

PURPOSE Wilms' tumor is a childhood cancer of the kidney with an incidence of approximately 1 in 10,000. Cooccurrence of Wilms' tumor with 2q37 deletion syndrome, an uncommon constitutional chromosome abnormality, has been reported previously in three children. Given these are independently rare clinical entities, we hypothesized that 2q37 harbors a tumor suppressor gene important in Wilms' tum...

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Human Cancer Biology Loss of Heterozygosity at 2q37 in Sporadic Wilms' Tumor: Putative Role for miR-562

Purpose: Wilms' tumor is a childhood cancer of the kidney with an incidence of ∼1 in 10,000. Cooccurrence of Wilms' tumor with 2q37 deletion syndrome, an uncommon constitutional chromosome abnormality, has been reported previously in three children. Given these are independently rare clinical entities, we hypothesized that 2q37 harbors a tumor suppressor gene important in Wilms' tumor pathogene...

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ژورنال

عنوان ژورنال: British Journal of Cancer

سال: 2000

ISSN: 0007-0920,1532-1827

DOI: 10.1054/bjoc.1999.0922