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Journal Abstract Search

182 related items for PubMed ID: 9425596

  • 1. Molecular genetics of Beckwith-Wiedemann syndrome.
    Li M, Squire JA, Weksberg R.
    Curr Opin Pediatr; 1997 Dec; 9(6):623-9. PubMed ID: 9425596
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  • 2. 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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  • 4. 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 15; 9(6):409-18. PubMed ID: 11436121
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  • 5. Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.
    Bachmann N, Crazzolara R, Bohne F, Kotzot D, Maurer K, Enklaar T, Prawitt D, Bergmann C.
    Pediatr Blood Cancer; 2017 Mar 15; 64(3):. PubMed ID: 27650505
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  • 6. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
    Soejima H, Higashimoto K.
    J Hum Genet; 2013 Jul 15; 58(7):402-9. PubMed ID: 23719190
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  • 7. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.
    Lee MP, Hu RJ, Johnson LA, Feinberg AP.
    Nat Genet; 1997 Feb 15; 15(2):181-5. PubMed ID: 9020845
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  • 9. Beckwith-Wiedemann syndrome.
    Weksberg R, Shuman C, Smith AC.
    Am J Med Genet C Semin Med Genet; 2005 Aug 15; 137C(1):12-23. PubMed ID: 16010676
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  • 12. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.
    Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voûte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, Westerveld A.
    Med Pediatr Oncol; 1996 Nov 15; 27(5):490-4. PubMed ID: 8827079
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  • 13. Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development.
    Weksberg R, Smith AC, Squire J, Sadowski P.
    Hum Mol Genet; 2003 Apr 01; 12 Spec No 1():R61-8. PubMed ID: 12668598
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  • 15. Genomic imprinting and Beckwith-Wiedemann syndrome.
    Hatada I, Mukai T.
    Histol Histopathol; 2000 Jan 01; 15(1):309-12. PubMed ID: 10668219
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  • 18. Growth regulation, imprinted genes, and chromosome 11p15.5.
    Smith AC, Choufani S, Ferreira JC, Weksberg R.
    Pediatr Res; 2007 May 01; 61(5 Pt 2):43R-47R. PubMed ID: 17413842
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