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Query Trace: Wilms Tumor and IGF2[orginal query]

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 Similar articles in PubMed
A high incidence of WT1 abnormality in bilateral Wilms tumours in Japan, and the penetrance rates in children with WT1 germline mutation. British journal of cancer 2015 Mar 112 (6): 1121-33. Kaneko Y, Okita H, Haruta M, Arai Y, Oue T, Tanaka Y, Horie H, Hinotsu S, Koshinaga T, Yoneda A, Ohtsuka Y, Taguchi T, Fukuzawa Similar articles in PubMed
Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children. Cancer science 2012 Jun 103 (6): 1129-35. Haruta Masayuki, Arai Yasuhito, Watanabe Naoki, Fujiwara Yuiko, Honda Shohei, Ohshima Junjiro, Kasai Fumio, Nakadate Hisaya, Horie Hiroshi, Okita Hajime, Hata Jun-Ichi, Fukuzawa Masahiro, Kaneko Yasuhi Similar articles in PubMed