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Journal Abstract Search

145 related items for PubMed ID: 10738297

  • 1. Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.
    Steenman M, Westerveld A, Mannens M.
    Genes Chromosomes Cancer; 2000 May; 28(1):1-13. PubMed ID: 10738297
    [Abstract] [Full Text] [Related]

  • 2. A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.
    Besnard-Guérin C, Newsham I, Winqvist R, Cavenee WK.
    Hum Genet; 1996 Feb; 97(2):163-70. PubMed ID: 8566947
    [Abstract] [Full Text] [Related]

  • 3. Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.
    Newsham I, Claussen U, Lüdecke HJ, Mason M, Senger G, Horsthemke B, Cavenee W.
    Genes Chromosomes Cancer; 1991 Mar; 3(2):108-16. PubMed ID: 1676905
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  • 6. Multiple genetic abnormalities of 11p15 in Wilms' tumor.
    Feinberg AP.
    Med Pediatr Oncol; 1996 Nov; 27(5):484-9. PubMed ID: 8827078
    [Abstract] [Full Text] [Related]

  • 7. Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma.
    Haas OA, Zoubek A, Grümayer ER, Gadner H.
    Cancer Genet Cytogenet; 1986 Oct; 23(2):95-104. PubMed ID: 3019515
    [Abstract] [Full Text] [Related]

  • 8. [Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome].
    Tsuchida Y, Yokomori K, Choi SH.
    Nihon Rinsho; 1995 Nov; 53(11):2742-8. PubMed ID: 8538037
    [Abstract] [Full Text] [Related]

  • 9. Molecular genetics of Wilms' tumour.
    Tay JS.
    J Paediatr Child Health; 1995 Oct; 31(5):379-83. PubMed ID: 8554853
    [Abstract] [Full Text] [Related]

  • 10. Beckwith-Wiedemann syndrome: clinical and etiopathogenic aspects of a model genomic imprinting entity.
    Cammarata-Scalisi F, Avendaño A, Stock F, Callea M, Sparago A, Riccio A.
    Arch Argent Pediatr; 2018 Oct 01; 116(5):368-373. PubMed ID: 30204990
    [Abstract] [Full Text] [Related]

  • 11. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M, Pelosse B, Laroche L, Vazquez MP.
    J Fr Ophtalmol; 2001 May 01; 24(5):479-81. PubMed ID: 11397983
    [Abstract] [Full Text] [Related]

  • 12. Decreased CDKN1C Expression in Congenital Alveolar Rhabdomyosarcoma Associated with Beckwith-Wiedemann Syndrome.
    Piersigilli F, Auriti C, Mondì V, Francalanci P, Salvatori G, Danhaive O.
    Indian J Pediatr; 2016 Nov 01; 83(12-13):1476-1478. PubMed ID: 27345568
    [Abstract] [Full Text] [Related]

  • 13. Beck-Wiedemann syndrome and Wilms' tumour.
    Ward A.
    Mol Hum Reprod; 1997 Feb 01; 3(2):157-68. PubMed ID: 9239720
    [Abstract] [Full Text] [Related]

  • 14. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
    Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, Okada A, Ohishi S, Nabetani A, Morisaki H, Nakayama M, Niikawa N, Mukai T.
    Nat Genet; 1996 Oct 01; 14(2):171-3. PubMed ID: 8841187
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 60(2):136-139. PubMed ID: 27965001
    [Abstract] [Full Text] [Related]

  • 16. Simultaneous Presentation of Wilms Tumor and Immature Ovarian Teratoma in Beckwith-Wiedemann Syndrome.
    White JC, Liu J, Nahar A.
    J Pediatr Hematol Oncol; 2018 Jan 01; 40(1):e61-e63. PubMed ID: 28692553
    [Abstract] [Full Text] [Related]

  • 17. Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.
    Little MH, Thomson DB, Hayward NK, Smith PJ.
    Hum Genet; 1988 Jun 01; 79(2):186-9. PubMed ID: 2839410
    [Abstract] [Full Text] [Related]

  • 18. Cytogenetics and molecular genetics of Wilms' tumor of childhood.
    Slater RM, Mannens MM.
    Cancer Genet Cytogenet; 1992 Jul 15; 61(2):111-21. PubMed ID: 1322233
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Diseases Predisposing to Adrenocortical Malignancy (Li-Fraumeni Syndrome, Beckwith-Wiedemann Syndrome, and Carney Complex).
    Jouinot A, Bertherat J.
    Exp Suppl; 2019 Nov 15; 111():149-169. PubMed ID: 31588532
    [Abstract] [Full Text] [Related]

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