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63. Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors. Yuan E; Li CM; Yamashiro DJ; Kandel J; Thaker H; Murty VV; Tycko B Mol Cancer Res; 2005 Sep; 3(9):493-502. PubMed ID: 16179496 [TBL] [Abstract][Full Text] [Related]
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65. Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma. el-Naggar AK; Lai S; Tucker SA; Clayman GL; Goepfert H; Hong WK; Huff V Oncogene; 1999 Nov; 18(50):7063-9. PubMed ID: 10597307 [TBL] [Abstract][Full Text] [Related]
66. IGF2 but not H19 shows loss of imprinting in human glioma. Uyeno S; Aoki Y; Nata M; Sagisaka K; Kayama T; Yoshimoto T; Ono T Cancer Res; 1996 Dec; 56(23):5356-9. PubMed ID: 8968084 [TBL] [Abstract][Full Text] [Related]
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68. Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. Reik W; Brown KW; Schneid H; Le Bouc Y; Bickmore W; Maher ER Hum Mol Genet; 1995 Dec; 4(12):2379-85. PubMed ID: 8634713 [TBL] [Abstract][Full Text] [Related]
69. Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer. Murrell A; Ito Y; Verde G; Huddleston J; Woodfine K; Silengo MC; Spreafico F; Perotti D; De Crescenzo A; Sparago A; Cerrato F; Riccio A PLoS One; 2008 Mar; 3(3):e1849. PubMed ID: 18365005 [TBL] [Abstract][Full Text] [Related]
70. Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome. Reik W; Maher ER Trends Genet; 1997 Aug; 13(8):330-4. PubMed ID: 9260520 [TBL] [Abstract][Full Text] [Related]
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72. Biallelic expression of the H19 and IGF2 genes in hepatocellular carcinoma. Kim KS; Lee YI Cancer Lett; 1997 Nov; 119(2):143-8. PubMed ID: 9570364 [TBL] [Abstract][Full Text] [Related]
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78. A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors. Newsham I; Kindler-Röhrborn A; Daub D; Cavenee W Genes Chromosomes Cancer; 1995 Jan; 12(1):1-7. PubMed ID: 7534105 [TBL] [Abstract][Full Text] [Related]
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80. Beckwith-Wiedemann syndrome. Choufani S; Shuman C; Weksberg R Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):343-54. PubMed ID: 20803657 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]