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Journal Abstract Search

167 related items for PubMed ID: 7843377

  • 1. Preliminary report of molecular detection of retinoblastoma gene mutations.
    Zeng R, Jiang X, Zhang Q, Hu B, Chen Y.
    Yan Ke Xue Bao; 1994 Mar; 10(1):1-5. PubMed ID: 7843377
    [Abstract] [Full Text] [Related]

  • 2. Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
    Lohmann DR, Gerick M, Brandt B, Oelschläger U, Lorenz B, Passarge E, Horsthemke B.
    Am J Hum Genet; 1997 Aug; 61(2):282-94. PubMed ID: 9311732
    [Abstract] [Full Text] [Related]

  • 3. Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.
    Kloss K, Währisch P, Greger V, Messmer E, Fritze H, Höpping W, Passarge E, Horsthemke B.
    Am J Med Genet; 1991 May 01; 39(2):196-200. PubMed ID: 2063924
    [Abstract] [Full Text] [Related]

  • 4. Molecular detection of constitutional deletions in patients with retinoblastoma.
    Blanquet V, Créau-Goldberg N, de Grouchy J, Turleau C.
    Am J Med Genet; 1991 Jun 01; 39(3):355-61. PubMed ID: 1867290
    [Abstract] [Full Text] [Related]

  • 5. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Jun 01; 33(1):53-61. PubMed ID: 23715307
    [Abstract] [Full Text] [Related]

  • 6. Loss of retinoblastoma gene and amplification of N-myc gene in retinoblastoma.
    Choi SW, Lee TW, Yang SW, Hong WS, Kim CM, Lee JO.
    J Korean Med Sci; 1993 Feb 01; 8(1):73-7. PubMed ID: 8343223
    [Abstract] [Full Text] [Related]

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  • 9. Mutations in the retinoblastoma gene and their expression in somatic and tumor cells of patients with hereditary retinoblastoma.
    Kato MV, Ishizaki K, Toguchida J, Kaneko A, Takayama J, Tanooka H, Kato T, Shimizu T, Sasaki MS.
    Hum Mutat; 1994 Feb 01; 3(1):44-51. PubMed ID: 8118465
    [Abstract] [Full Text] [Related]

  • 10. Constitutional nonsense germline mutations in the RB1 gene detected in patients with early onset unilateral retinoblastoma.
    Cowell JK, Cragg H.
    Eur J Cancer; 1996 Sep 01; 32A(10):1749-52. PubMed ID: 8983285
    [Abstract] [Full Text] [Related]

  • 11. RB1 gene mutations in retinoblastoma.
    Lohmann DR.
    Hum Mutat; 1999 Sep 01; 14(4):283-8. PubMed ID: 10502774
    [Abstract] [Full Text] [Related]

  • 12. Retinoblastoma.
    Ponz de Leon M.
    Recent Results Cancer Res; 1994 Sep 01; 136():59-67. PubMed ID: 7863107
    [No Abstract] [Full Text] [Related]

  • 13. Molecular diagnosis in patients with retinoblastoma: Report of a series of cases.
    Ossandón D, Zanolli M, López JP, Benavides F, Pérez V, Repetto GM.
    Arch Soc Esp Oftalmol; 2016 Aug 01; 91(8):379-84. PubMed ID: 27021801
    [Abstract] [Full Text] [Related]

  • 14. Detection of tumor suppressor gene and oncogene in So-Rb50 human retinoblastoma cell line.
    Wang X, Zeng F, Xu Z, Zheng Y, Wang L.
    Yan Ke Xue Bao; 1993 Mar 01; 9(1):34-7. PubMed ID: 8253182
    [Abstract] [Full Text] [Related]

  • 15. [Prediction of retinoblastoma: linkage analysis of families with hereditary retinoblastoma by using polymorphic sites within the Rb gene].
    Yuan L, Gao Y, Lo S, Fang B, Ye J.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Oct 01; 17(5):338-42. PubMed ID: 8706167
    [Abstract] [Full Text] [Related]

  • 16. An association of the RB gene with osteosarcoma: molecular genetic evaluation of a case of hereditary retinoblastoma.
    Issing WJ, Wustrow TP, Oeckler R, Mezger J, Nerlich A.
    Eur Arch Otorhinolaryngol; 1993 Oct 01; 250(5):277-80. PubMed ID: 8217129
    [Abstract] [Full Text] [Related]

  • 17. Constitutional deletions predisposing to retinoblastoma.
    Janson M, Kock E, Nordenskjöld M.
    Hum Genet; 1990 Jun 01; 85(1):21-4. PubMed ID: 1972694
    [Abstract] [Full Text] [Related]

  • 18. Retinoblastoma.
    Lueder GT, Smith ME.
    Semin Diagn Pathol; 1994 May 01; 11(2):104-6. PubMed ID: 7809503
    [Abstract] [Full Text] [Related]

  • 19. Detection of mutations in the RB1 gene by single strand conformation polymorphism (SSCP) analysis, amplification mismatch detection (AMD) analysis and polymerase chain reaction sequencing.
    Dundar M, Lanyon GW, Connor MJ.
    Proc Natl Sci Counc Repub China B; 2001 Jul 01; 25(3):166-73. PubMed ID: 11480772
    [Abstract] [Full Text] [Related]

  • 20. Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.
    Brichard B, Heusterspreute M, De Potter P, Chantrain C, Vermylen C, Sibille C, Gala JL.
    Eur J Cancer; 2006 Jan 01; 42(1):65-72. PubMed ID: 16343894
    [Abstract] [Full Text] [Related]

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