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311 related items for PubMed ID: 2568588

  • 1. Preferential germline mutation of the paternal allele in retinoblastoma.
    Zhu XP, Dunn JM, Phillips RA, Goddard AD, Paton KE, Becker A, Gallie BL.
    Nature; 1989 Jul 27; 340(6231):312-3. PubMed ID: 2568588
    [Abstract] [Full Text] [Related]

  • 2. Parental origin of mutations of the retinoblastoma gene.
    Dryja TP, Mukai S, Petersen R, Rapaport JM, Walton D, Yandell DW.
    Nature; 1989 Jun 15; 339(6225):556-8. PubMed ID: 2733786
    [Abstract] [Full Text] [Related]

  • 3. Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma.
    Toguchida J, Ishizaki K, Sasaki MS, Ikenaga M, Sugimoto M, Kotoura Y, Yamamuro T.
    Cancer Res; 1988 Jul 15; 48(14):3939-43. PubMed ID: 2898286
    [Abstract] [Full Text] [Related]

  • 4. A molecular study of first and second RB1 mutational hits in retinoblastoma patients.
    de Andrade AF, da Hora Barbosa R, Vargas FR, Ferman S, Eisenberg AL, Fernandes L, Bonvicino CR.
    Cancer Genet Cytogenet; 2006 May 15; 167(1):43-6. PubMed ID: 16682285
    [Abstract] [Full Text] [Related]

  • 5. The genetics of retinoblastoma.
    Stahl A, Levy N, Wadzynska T, Sussan JM, Jourdan-Fonta D, Saracco JB.
    Ann Genet; 1994 May 15; 37(4):172-8. PubMed ID: 7710251
    [Abstract] [Full Text] [Related]

  • 6. Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling.
    Munier FL, Thonney F, Balmer A, Héon E, Pescia G, Schorderet DF.
    Klin Monbl Augenheilkd; 1996 May 15; 208(5):400-3. PubMed ID: 8766064
    [Abstract] [Full Text] [Related]

  • 7. 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 15; 42(1):65-72. PubMed ID: 16343894
    [Abstract] [Full Text] [Related]

  • 8. Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma.
    Toguchida J, Ishizaki K, Sasaki MS, Nakamura Y, Ikenaga M, Kato M, Sugimot M, Kotoura Y, Yamamuro T.
    Nature; 1989 Mar 09; 338(6211):156-8. PubMed ID: 2918936
    [Abstract] [Full Text] [Related]

  • 9. RB1 gene mutations in retinoblastoma.
    Lohmann DR.
    Hum Mutat; 1999 Mar 09; 14(4):283-8. PubMed ID: 10502774
    [Abstract] [Full Text] [Related]

  • 10. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
    Nichols KE, Houseknecht MD, Godmilow L, Bunin G, Shields C, Meadows A, Ganguly A.
    Hum Mutat; 2005 Jun 09; 25(6):566-74. PubMed ID: 15884040
    [Abstract] [Full Text] [Related]

  • 11. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Jun 09; 33(1):53-61. PubMed ID: 23715307
    [Abstract] [Full Text] [Related]

  • 12. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.
    Choy KW, Pang CP, Yu CB, Wong HL, Ng JS, Fan DS, Lo KW, Chai JT, Wang J, Fu W, Lam DS.
    Hum Mutat; 2002 Nov 09; 20(5):408. PubMed ID: 12402348
    [Abstract] [Full Text] [Related]

  • 13. Identification of four novel RB1 germline mutations in Korean retinoblastoma patients.
    Yu YS, Kim IJ, Ku JL, Park JG.
    Hum Mutat; 2001 Sep 09; 18(3):252. PubMed ID: 11524739
    [Abstract] [Full Text] [Related]

  • 14. Preferential retention of paternal alleles in human retinoblastoma: evidence for genomic imprinting.
    Leach RJ, Magewu AN, Buckley JD, Benedict WF, Rother C, Murphree AL, Griegel S, Rajewsky MF, Jones PA.
    Cell Growth Differ; 1990 Sep 09; 1(9):401-6. PubMed ID: 1981144
    [Abstract] [Full Text] [Related]

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  • 16. The molecular genetics of retinoblastoma.
    Goodrich DW, Lee WH.
    Cancer Surv; 1990 Sep 09; 9(3):529-54. PubMed ID: 2101724
    [Abstract] [Full Text] [Related]

  • 17. Detection of mosaic RB1 mutations in families with retinoblastoma.
    Rushlow D, Piovesan B, Zhang K, Prigoda-Lee NL, Marchong MN, Clark RD, Gallie BL.
    Hum Mutat; 2009 May 09; 30(5):842-51. PubMed ID: 19280657
    [Abstract] [Full Text] [Related]

  • 18. Genome instability in secondary solid tumors developing after radiotherapy of bilateral retinoblastoma.
    Lefèvre SH, Vogt N, Dutrillaux AM, Chauveinc L, Stoppa-Lyonnet D, Doz F, Desjardins L, Dutrillaux B, Chevillard S, Malfoy B.
    Oncogene; 2001 Dec 06; 20(56):8092-9. PubMed ID: 11781822
    [Abstract] [Full Text] [Related]

  • 19. Improved clinical management of retinoblastoma through gene testing.
    Raizis A, Clemett R, Corbett R, McGaughran J, Evans J, George P.
    N Z Med J; 2002 May 24; 115(1154):231-4. PubMed ID: 12117173
    [Abstract] [Full Text] [Related]

  • 20. Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin effect.
    Schüler A, Weber S, Neuhäuser M, Jurklies C, Lehnert T, Heimann H, Rudolph G, Jöckel KH, Bornfeld N, Lohmann DR.
    Eur J Cancer; 2005 Mar 24; 41(5):735-40. PubMed ID: 15763650
    [Abstract] [Full Text] [Related]

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