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165 related items for PubMed ID: 16252245

  • 1. 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; 77(5):887-91. PubMed ID: 16252245
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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. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
    Weksberg R, Nishikawa J, Caluseriu O, Fei YL, Shuman C, Wei C, Steele L, Cameron J, Smith A, Ambus I, Li M, Ray PN, Sadowski P, Squire J.
    Hum Mol Genet; 2001 Dec 15; 10(26):2989-3000. PubMed ID: 11751681
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  • 5. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.
    DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP.
    Am J Hum Genet; 2002 Mar 15; 70(3):604-11. PubMed ID: 11813134
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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 15; 65(10):e27296. PubMed ID: 29932284
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  • 12. Calcifying nested stromal-epithelial tumor (CNSET) of the liver in Beckwith-Wiedemann syndrome.
    Khoshnam N, Robinson H, Clay MR, Schaffer LR, Gillespie SE, Shehata BM.
    Eur J Med Genet; 2017 Feb 15; 60(2):136-139. PubMed ID: 27965001
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  • 13. Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.
    Sparago A, Russo S, Cerrato F, Ferraiuolo S, Castorina P, Selicorni A, Schwienbacher C, Negrini M, Ferrero GB, Silengo MC, Anichini C, Larizza L, Riccio A.
    Hum Mol Genet; 2007 Feb 01; 16(3):254-64. PubMed ID: 17158821
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  • 16. Molecular biology of Beckwith-Wiedemann syndrome.
    Weksberg R, Squire JA.
    Med Pediatr Oncol; 1996 Nov 01; 27(5):462-9. PubMed ID: 8827075
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  • 17. A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS).
    Janchevska A, Tasic V, Laban N, Polenakovic M, Gucev Z, Bachmann N, Bergmann C.
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2018 Dec 01; 39(2-3):131-135. PubMed ID: 30864369
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  • 20. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
    Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, Grundy R, Bowdin SC, Riccio A, Sebastio G, Bliek J, Schofield PN, Reik W, Macdonald F, Maher ER.
    Eur J Hum Genet; 2005 Sep 01; 13(9):1025-32. PubMed ID: 15999116
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