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Journal Abstract Search

231 related items for PubMed ID: 3037545

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  • 24. Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.
    Drechsler M, Meijers-Heijboer EJ, Schneider S, Schurich B, Grond-Ginsbach C, Tariverdian G, Kantner G, Blankenagel A, Kaps D, Schroeder-Kurth T.
    Hum Genet; 1994 Oct; 94(4):331-8. PubMed ID: 7927324
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  • 25. 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
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  • 26. A mouse model of the aniridia-Wilms tumor deletion syndrome.
    Glaser T, Lane J, Housman D.
    Science; 1990 Nov 09; 250(4982):823-7. PubMed ID: 2173141
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  • 27. Wilms tumour: a developmental anomaly.
    Hastie ND, Bickmore W, Pritchard-Jones K, Porteous DJ, van Heyningen V.
    Princess Takamatsu Symp; 1989 Nov 09; 20():145-50. PubMed ID: 2562179
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  • 29. The E7-associated cell-surface antigen: a marker for the 11p13 chromosomal deletion associated with aniridia-Wilms tumor.
    Scoggin CH, Fisher JH, Shoemaker SA, Morse H, Leigh T, Riccardi VM.
    Am J Hum Genet; 1985 Sep 09; 37(5):883-9. PubMed ID: 2996335
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  • 30. Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
    Crolla JA, van Heyningen V.
    Am J Hum Genet; 2002 Nov 09; 71(5):1138-49. PubMed ID: 12386836
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  • 31. Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping.
    Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA.
    Nature; 1990 Feb 22; 343(6260):774-8. PubMed ID: 2154702
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  • 32. A sequence-ready 3-Mb PAC contig covering 16 breakpoints of the Wilms tumor/anirida region of human chromosome 11p13.
    Niederführ A, Hummerich H, Gawin B, Boyle S, Little PF, Gessler M.
    Genomics; 1998 Oct 15; 53(2):155-63. PubMed ID: 9790764
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  • 37. The Wilms tumour (WT1) gene is mutated in a secondary leukaemia in a WAGR patient.
    Pritchard-Jones K, Renshaw J, King-Underwood L.
    Hum Mol Genet; 1994 Sep 15; 3(9):1633-7. PubMed ID: 7833922
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  • 39. The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus.
    Boehm T, Lavenir I, Forster A, Wadey RB, Cowell JK, Harbott J, Lampert F, Waters J, Sherrington P, Couillin P.
    Oncogene; 1988 Dec 15; 3(6):691-5. PubMed ID: 2577871
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