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276 related items for PubMed ID: 2539717

  • 1. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
    Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, Lampkin BC, Kalbakji A, Cavenee WK.
    Am J Hum Genet; 1989 May; 44(5):711-9. PubMed ID: 2539717
    [Abstract] [Full Text] [Related]

  • 2. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
    Grundy P, Koufos A, Morgan K, Li FP, Meadows AT, Cavenee WK.
    Nature; 1988 Nov 24; 336(6197):374-6. PubMed ID: 2848199
    [Abstract] [Full Text] [Related]

  • 3. 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 24; 12(1):1-7. PubMed ID: 7534105
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  • 4. Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.
    Barr CL, Best L, Weksberg R.
    Am J Med Genet; 2001 Nov 22; 104(2):120-6. PubMed ID: 11746041
    [Abstract] [Full Text] [Related]

  • 5. [Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome].
    Tsuchida Y, Yokomori K, Choi SH.
    Nihon Rinsho; 1995 Nov 22; 53(11):2742-8. PubMed ID: 8538037
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 15; 97(2):163-70. PubMed ID: 8566947
    [Abstract] [Full Text] [Related]

  • 8. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.
    Reeve AE, Sih SA, Raizis AM, Feinberg AP.
    Mol Cell Biol; 1989 Apr 15; 9(4):1799-803. PubMed ID: 2542777
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  • 11. Frequency of WT1 and 11p15 constitutional aberrations and phenotypic correlation in childhood Wilms tumour patients.
    Segers H, Kersseboom R, Alders M, Pieters R, Wagner A, van den Heuvel-Eibrink MM.
    Eur J Cancer; 2012 Nov 15; 48(17):3249-56. PubMed ID: 22796116
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  • 12. Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.
    Henry I, Grandjouan S, Couillin P, Barichard F, Huerre-Jeanpierre C, Glaser T, Philip T, Lenoir G, Chaussain JL, Junien C.
    Proc Natl Acad Sci U S A; 1989 May 15; 86(9):3247-51. PubMed ID: 2566168
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  • 13. Multiple genetic abnormalities of 11p15 in Wilms' tumor.
    Feinberg AP.
    Med Pediatr Oncol; 1996 Nov 15; 27(5):484-9. PubMed ID: 8827078
    [Abstract] [Full Text] [Related]

  • 14. Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.
    Couillin P, Azoulay M, Henry I, Ravisé N, Grisard MC, Jeanpierre C, Barichard F, Metezeau P, Candelier JJ, Lewis W.
    Hum Genet; 1989 May 15; 82(2):171-8. PubMed ID: 2722195
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  • 15. 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 15; 23(2):95-104. PubMed ID: 3019515
    [Abstract] [Full Text] [Related]

  • 16. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.
    Glaser T, Lewis WH, Bruns GA, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KO.
    Nature; 1986 Oct 15; 321(6073):882-7. PubMed ID: 3014343
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  • 17. Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers.
    Bickmore W, Christie S, van Heyningen V, Hastie ND, Porteous DJ.
    Nucleic Acids Res; 1988 Jan 11; 16(1):51-60. PubMed ID: 2829125
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  • 19. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.
    Ping AJ, Reeve AE, Law DJ, Young MR, Boehnke M, Feinberg AP.
    Am J Hum Genet; 1989 May 11; 44(5):720-3. PubMed ID: 2565083
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  • 20. The M1 subunit of ribonucleotide reductase refines mapping of genetic rearrangements at chromosome 11p15.
    Byrne JA, Little MH, Smith PJ.
    Cancer Genet Cytogenet; 1992 Apr 11; 59(2):206-9. PubMed ID: 1316226
    [Abstract] [Full Text] [Related]

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