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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Query Trace: Familial Wilms Tumor 2[original query]
Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor.
Nature genetics 2008 Nov 40 (11): 1329-34.
Scott Richard H, Douglas Jenny, Baskcomb Linda, Huxter Nikki, Barker Karen, Hanks Sandra, Craft Alan, Gerrard Mary, Kohler Janice A, Levitt Gill A, Picton Sue, Pizer Barry, Ronghe Milind D, Williams Denise, , Cook Jackie A, Pujol Pascal, Maher Eamonn R, Birch Jillian M, Stiller Charles A, Pritchard-Jones Kathy, Rahman Nazne
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