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

PURPOSE: Wilms tumor is a childhood cancer of the kidney with an incidence of ~1 in 10,000. Co-occurrence of Wilms tumor with 2q37 deletion syndrome, an uncommon constitutional chromosome abnormality, has previously been reported in three children. Given these are independently rare clinical entitie...

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Detalhes bibliográficos
Main Authors: Drake, Kylie M., Ruteshouser, E Cristy, Natrajan, Rachael, Harbor, Phyllis, Wegert, Jenny, Gessler, Manfred, Pritchard-Jones, Kathy, Grundy, Paul, Dome, Jeffrey, Huff, Vicki, Jones, Chris, Aldred, Micheala A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2756455/
https://ncbi.nlm.nih.gov/pubmed/19789318
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1078-0432.CCR-09-1065
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