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Journal Abstract Search

170 related items for PubMed ID: 1769647

  • 21. Molecular analysis of chromosome region 11p13 in patients with Drash syndrome.
    Jadresic L, Wadey RB, Buckle B, Barratt TM, Mitchell CD, Cowell JK.
    Hum Genet; 1991 Mar; 86(5):497-501. PubMed ID: 1849870
    [Abstract] [Full Text] [Related]

  • 22. A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
    Crolla JA, Cawdery JE, Oley CA, Young ID, Gray J, Fantes J, van Heyningen V.
    J Med Genet; 1997 Mar; 34(3):207-12. PubMed ID: 9132491
    [Abstract] [Full Text] [Related]

  • 23. Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome.
    Gessler M, König A, Moore J, Qualman S, Arden K, Cavenee W, Bruns G.
    Genes Chromosomes Cancer; 1993 Jul; 7(3):131-6. PubMed ID: 7687865
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  • 24. Evaluation of chromosome 11p imbalances in aniridia and Wilms tumor patients.
    Busch M, Leube B, Thiel A, Schanze I, Beier M, Royer-Pokora B.
    Am J Med Genet A; 2013 May; 161A(5):958-64. PubMed ID: 23494989
    [Abstract] [Full Text] [Related]

  • 25. 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; 3(9):1633-7. PubMed ID: 7833922
    [Abstract] [Full Text] [Related]

  • 26. Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion.
    van Heyningen V, Hoovers JM, de Kraker J, Crolla JA.
    J Med Genet; 2007 Dec; 44(12):787-90. PubMed ID: 17630404
    [Abstract] [Full Text] [Related]

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  • 28. Molecular analysis of chromosomal rearrangements using pulsed field gel electrophoresis and somatic cell hybrids.
    Davis LM.
    Environ Mol Mutagen; 1991 Dec; 18(4):263-9. PubMed ID: 1660807
    [Abstract] [Full Text] [Related]

  • 29. Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
    Gessler M, Bruns GA.
    Genomics; 1988 Aug; 3(2):117-23. PubMed ID: 2852160
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  • 31. Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias.
    Lorda-Sanchez I, Sanz R, Diaz-Guillen MA, Fernandez-Toral J, Heine-Suñer D, Rodriguez De Alba M, Gonzalez-Gonzalez C, Trujillo MJ, Ramos C, Rodriguez De Cordoba S, Ayuso C.
    Genet Couns; 2002 Aug; 13(2):171-7. PubMed ID: 12150218
    [Abstract] [Full Text] [Related]

  • 32. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome.
    Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D.
    Genomics; 1989 Nov; 5(4):880-93. PubMed ID: 2574149
    [Abstract] [Full Text] [Related]

  • 33. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.
    Kaneko Y, Homma C, Maseki N, Sakurai M, Hata J.
    Cancer Res; 1991 Nov 01; 51(21):5937-42. PubMed ID: 1657374
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  • 36. Aniridia, Wilms' tumor and human chromosome 11.
    Bickmore WA, Hastie ND.
    Ophthalmic Paediatr Genet; 1989 Dec 01; 10(4):229-48. PubMed ID: 2560823
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  • 37. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
    Davis LM, Stallard R, Thomas GH, Couillin P, Junien C, Nowak NJ, Shows TB.
    Science; 1988 Aug 12; 241(4867):840-2. PubMed ID: 2841760
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  • 39. 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]

  • 40. Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene.
    Rose EA, Glaser T, Jones C, Smith CL, Lewis WH, Call KM, Minden M, Champagne E, Bonetta L, Yeger H.
    Cell; 1990 Feb 09; 60(3):495-508. PubMed ID: 2154334
    [Abstract] [Full Text] [Related]

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