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199 related items for PubMed ID: 38142265

  • 1. Cancer predisposition signaling in Beckwith-Wiedemann Syndrome drives Wilms tumor development.
    Nirgude S, Naveh NSS, Kavari SL, Traxler EM, Kalish JM.
    Br J Cancer; 2024 Mar; 130(4):638-650. PubMed ID: 38142265
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  • 2. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
    Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C.
    Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
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  • 3. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.
    O'Keefe D, Dao D, Zhao L, Sanderson R, Warburton D, Weiss L, Anyane-Yeboa K, Tycko B.
    Am J Hum Genet; 1997 Aug; 61(2):295-303. PubMed ID: 9311733
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  • 4. Concurrent Hepatoblastoma and Wilms Tumor Leading to Diagnosis of Beckwith-Wiedemann Syndrome.
    Wolfe DM, Webster Carrion A, Masukhani MM, Oberg JA, Pavisic J, El-Ali A, Gupta M, Weng K, Glasser CL.
    J Pediatr Hematol Oncol; 2023 May 01; 45(4):e525-e529. PubMed ID: 36730589
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  • 5. 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 01; 12(1):1-7. PubMed ID: 7534105
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  • 6. Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor.
    MacFarland SP, Duffy KA, Bhatti TR, Bagatell R, Balamuth NJ, Brodeur GM, Ganguly A, Mattei PA, Surrey LF, Balis FM, Kalish JM.
    Pediatr Blood Cancer; 2018 Oct 01; 65(10):e27296. PubMed ID: 29932284
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  • 7. Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.
    Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR.
    Am J Hum Genet; 2005 Nov 01; 77(5):887-91. PubMed ID: 16252245
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  • 8. Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS).
    Bliek J, Gicquel C, Maas S, Gaston V, Le Bouc Y, Mannens M.
    J Pediatr; 2004 Dec 01; 145(6):796-9. PubMed ID: 15580204
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  • 10. Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith-Wiedemann syndrome.
    Sobel Naveh NS, Traxler EM, Duffy KA, Kalish JM.
    Hepatol Commun; 2022 Aug 01; 6(8):2132-2146. PubMed ID: 35507738
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  • 20. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.
    Lin HY, Chuang CK, Tu RY, Fang YY, Su YN, Chen CP, Chang CY, Liu HC, Chu TH, Niu DM, Lin SP.
    Mol Genet Metab; 2016 Sep 01; 119(1-2):8-13. PubMed ID: 27436784
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