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Journal Abstract Search

184 related items for PubMed ID: 2154698

  • 1. Molecular genetics. A gene for Wilms tumour?
    Francke U.
    Nature; 1990 Feb 22; 343(6260):692-4. PubMed ID: 2154698
    [No Abstract] [Full Text] [Related]

  • 2. Wilms' tumour and related syndromes. A unifying theory.
    Côté GB.
    Ann Genet; 1989 Feb 22; 32(2):69-72. PubMed ID: 2547332
    [Abstract] [Full Text] [Related]

  • 3. Retinoblastoma--genetic insights into neoplasia.
    Nyhan WL.
    Bioessays; 1987 Jan 22; 6(1):5-8. PubMed ID: 2882750
    [No Abstract] [Full Text] [Related]

  • 4. Genetics of embryonal tumours of childhood: retinoblastoma, Wilms' tumour and neuroblastoma.
    Brodeur GM.
    Cancer Surv; 1995 Jan 22; 25():67-99. PubMed ID: 8718513
    [Abstract] [Full Text] [Related]

  • 5. [Cytogenetics of malignant neoplasms].
    Pogosiants EE.
    Vopr Onkol; 1985 Jan 22; 31(8):92-101. PubMed ID: 2994300
    [No Abstract] [Full Text] [Related]

  • 6. The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivity.
    Sabatier L, Hoffschir F, al Achkar WA, Turleau C, de Grouchy J, Dutrillaux B.
    Ann Genet; 1989 Jan 22; 32(3):144-8. PubMed ID: 2554783
    [Abstract] [Full Text] [Related]

  • 7. The significance of genetic research in ophthalmology.
    Francois J.
    Birth Defects Orig Artic Ser; 1982 Jan 22; 18(6):3-25. PubMed ID: 6293603
    [No Abstract] [Full Text] [Related]

  • 8. Contribution and mechanisms of genetic predisposition to cancer: hereditary cancers and anti-oncogenes.
    Knudson AG.
    Prog Clin Biol Res; 1983 Jan 22; 132C():351-60. PubMed ID: 6314359
    [No Abstract] [Full Text] [Related]

  • 9. Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories.
    de Grouchy J.
    Prog Clin Biol Res; 1982 Jan 22; 103 Pt B():359-67. PubMed ID: 6298811
    [Abstract] [Full Text] [Related]

  • 10. [Genetics and cancer].
    Cardesa JJ, Blesa E, Durán J, Moreno F, Espinosa J, Zarallo L.
    An Esp Pediatr; 1985 Aug 22; 23(2):116-22. PubMed ID: 2998249
    [No Abstract] [Full Text] [Related]

  • 11. 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]

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  • 14. Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma.
    Punnett A, Teshima I, Heon E, Budning A, Sutherland J, Gallie BL, Chan HS.
    Am J Med Genet A; 2003 Jul 01; 120A(1):105-9. PubMed ID: 12794701
    [Abstract] [Full Text] [Related]

  • 15. The chromosome 11 region flanking the t(11;14) breakpoint in human T-ALL is deleted in Wilms' tumor hybrids.
    Finver SN, Martiniere C, Kagan J, Cavenee W, Croce CM.
    Oncogene Res; 1989 Jul 01; 5(2):143-8. PubMed ID: 2558334
    [Abstract] [Full Text] [Related]

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  • 17. Infrequent mutation of the WT1 gene in 77 Wilms' Tumors.
    Gessler M, König A, Arden K, Grundy P, Orkin S, Sallan S, Peters C, Ruyle S, Mandell J, Li F.
    Hum Mutat; 1994 Jul 01; 3(3):212-22. PubMed ID: 8019557
    [Abstract] [Full Text] [Related]

  • 18. Mutation and cancer: a model for Wilms' tumor of the kidney.
    Knudson AG, Strong LC.
    J Natl Cancer Inst; 1972 Feb 01; 48(2):313-24. PubMed ID: 4347033
    [No Abstract] [Full Text] [Related]

  • 19. Molecular mechanisms in familial and sporadic cancers.
    Lancet; 1988 Jan 16; 1(8577):92-4. PubMed ID: 2891986
    [No Abstract] [Full Text] [Related]

  • 20. [Tumor suppressor genes: occurrence, significance and function].
    Scheurlen W, Kreth HW.
    Monatsschr Kinderheilkd; 1991 Oct 16; 139(10):650-4. PubMed ID: 1660097
    [Abstract] [Full Text] [Related]

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