Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Wilms Tumor and H19[original query] |
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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 |
Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups. American journal of medical genetics. Part A 2016 Jul . Maas Saskia M, Vansenne Fleur, Kadouch Daniel J M, Ibrahim Abdulla, Bliek Jet, Hopman Saskia, Mannens Marcel M, Merks Johannes H M, Maher Eamonn R, Hennekam Raoul |
H19 gene polymorphisms and Wilms tumor risk in Chinese children: a four-center case-control study. Molecular genetics & genomic medicine 2021 Jan e1584. Li Wenya, Hua Rui-Xi, Wang Mi, Zhang Da, Zhu Jinhong, Zhang Songyang, Yang Yang, Cheng Jiwen, Zhou Haixia, Zhang Jiao, He Ji |
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