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    Results: 1 to 20 of 151

    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.PMID: 2539717 [PubMed - indexed for MEDLINE]Related articlesFree article

    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.PMID: 2848199 [PubMed - indexed for MEDLINE]Related articles

    3.

    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.PMID: 11746041 [PubMed - indexed for MEDLINE]Related articles

    4.

    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;12(1):1-7.PMID: 7534105 [PubMed - indexed for MEDLINE]Related articles

    5.

    Cytogenetics and molecular genetics of Wilms' tumor of childhood.

    Slater RM, Mannens MM.

    Cancer Genet Cytogenet. 1992 Jul 15;61(2):111-21. Review.PMID: 1322233 [PubMed - indexed for MEDLINE]Related articles

    6.

    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.PMID: 8566947 [PubMed - indexed for MEDLINE]Related articles

    7.

    [Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome]

    Tsuchida Y, Yokomori K, Choi SH.

    Nippon Rinsho. 1995 Nov;53(11):2742-8. Review. Japanese. PMID: 8538037 [PubMed - indexed for MEDLINE]Related articles

    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;9(4):1799-803.PMID: 2542777 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    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.PMID: 1676905 [PubMed - indexed for MEDLINE]Related articles

    10.

    Molecular genetics of Wilms' tumour.

    Tay JS.

    J Paediatr Child Health. 1995 Oct;31(5):379-83. Review.PMID: 8554853 [PubMed - indexed for MEDLINE]Related articles

    11.

    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;86(9):3247-51.PMID: 2566168 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    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, et al.

    Hum Genet. 1989 May;82(2):171-8.PMID: 2722195 [PubMed - indexed for MEDLINE]Related articles

    13.

    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, et al.

    Nature. 1986 Jun 26-Jul 2;321(6073):882-7.PMID: 3014343 [PubMed - indexed for MEDLINE]Related articles

    14.

    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.PMID: 3019515 [PubMed - indexed for MEDLINE]Related articles

    15.

    Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination.

    Coppes MJ, Bonetta L, Huang A, Hoban P, Chilton-MacNeill S, Campbell CE, Weksberg R, Yeger H, Reeve AE, Williams BR.

    Genes Chromosomes Cancer. 1992 Nov;5(4):326-34. Review.PMID: 1283321 [PubMed - indexed for MEDLINE]Related articles

    16.

    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 1;16(3):254-64. Epub 2006 Dec 11.PMID: 17158821 [PubMed - indexed for MEDLINE]Related articlesFree article

    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.PMID: 2829125 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Multiple genetic abnormalities of 11p15 in Wilms' tumor.

    Feinberg AP.

    Med Pediatr Oncol. 1996 Nov;27(5):484-9. Review.PMID: 8827078 [PubMed - indexed for MEDLINE]Related articles

    19.

    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.PMID: 9311733 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan.

    Kaneko Y, Takeda O, Homma C, Maseki N, Miyoshi H, Tsunematsu Y, Williams BG, Saunders GF, Sakurai M.

    Jpn J Cancer Res. 1993 Jun;84(6):616-24.PMID: 8393432 [PubMed - indexed for MEDLINE]Related articles

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