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Journal Abstract Search

212 related items for PubMed ID: 7687865

  • 21. Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
    Crolla JA, van Heyningen V.
    Am J Hum Genet; 2002 Nov; 71(5):1138-49. PubMed ID: 12386836
    [Abstract] [Full Text] [Related]

  • 22. 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. PubMed ID: 2542777
    [Abstract] [Full Text] [Related]

  • 23. The role of Wilms' tumor genes.
    Hirose M.
    J Med Invest; 1999 Aug; 46(3-4):130-40. PubMed ID: 10687307
    [Abstract] [Full Text] [Related]

  • 24. Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11.
    Compton DA, Weil MM, Jones C, Riccardi VM, Strong LC, Saunders GF.
    Cell; 1988 Dec 02; 55(5):827-36. PubMed ID: 2847871
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  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Cell types expressing the Wilms' tumour gene (WT1) in Wilms' tumours: implications for tumour histogenesis.
    Pritchard-Jones K, Fleming S.
    Oncogene; 1991 Dec 22; 6(12):2211-20. PubMed ID: 1722569
    [Abstract] [Full Text] [Related]

  • 27. De novo chromosome translocation t (2; 11) (p25.1; p13) in a patient with aniridia and genitourinary abnormalities.
    Hung HM, Lin SC, Su PH, Chen JY.
    Acta Paediatr Taiwan; 2003 Dec 22; 44(2):101-3. PubMed ID: 12845852
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  • 31. LMO2 gene deletions significantly worsen the prognosis of Wilms' tumor development in patients with WAGR syndrome.
    Marakhonov AV, Vasilyeva TA, Voskresenskaya AA, Sukhanova NV, Kadyshev VV, Kutsev SI, Zinchenko RA.
    Hum Mol Genet; 2019 Oct 01; 28(19):3323-3326. PubMed ID: 31304537
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  • 33. Congenital diaphragmatic hernia in WAGR syndrome.
    Scott DA, Cooper ML, Stankiewicz P, Patel A, Potocki L, Cheung SW.
    Am J Med Genet A; 2005 May 01; 134(4):430-3. PubMed ID: 15779010
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  • 34. [Nephroblastoma (Wilms' tumor): cytogenetic and molecular biology principles].
    Strohmeyer T.
    Klin Padiatr; 1993 May 01; 205(3):135-9. PubMed ID: 8394474
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  • 36. 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
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  • 38. Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases.
    Wang Q, Zhang X, Qin T, Wang D, Lin X, Zhu Y, Tan H, Zhao L, Li J, Lin Z, Lin H, Chen W.
    Genes (Basel); 2022 Aug 12; 13(8):. PubMed ID: 36011342
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  • 40. 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 12; 84(6):616-24. PubMed ID: 8393432
    [Abstract] [Full Text] [Related]

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