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137 related items for PubMed ID: 11277399

  • 1. A microsatellite fluorescent method for linkage analysis in familial retinoblastoma and deletion detection at the RB1 locus in retinoblastoma and osteosarcoma.
    Alonso J, García-Miguel P, Abelairas J, Mendiola M, Pestaña A.
    Diagn Mol Pathol; 2001 Mar; 10(1):9-14. PubMed ID: 11277399
    [Abstract] [Full Text] [Related]

  • 2. Prediction of retinoblastoma and osteosarcoma: linkage analysis of families by using polymorphic markers around RB1 locus.
    Chunder N, Basu D, Roy A, Roychoudhury S, Panda CK.
    J BUON; 2003 Mar; 8(4):365-9. PubMed ID: 17472278
    [Abstract] [Full Text] [Related]

  • 3. RB1 germ-line deletions in Argentine retinoblastoma patients.
    Fernández C, Repetto K, Dalamon V, Bergonzi F, Ferreiro V, Szijan I.
    Mol Diagn Ther; 2007 Mar; 11(1):55-61. PubMed ID: 17286450
    [Abstract] [Full Text] [Related]

  • 4. Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
    Ramprasad VL, Madhavan J, Murugan S, Sujatha J, Suresh S, Sharma T, Kumaramanickavel G.
    Mol Diagn Ther; 2007 Mar; 11(1):63-70. PubMed ID: 17286451
    [Abstract] [Full Text] [Related]

  • 5. First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.
    Girardet A, Hamamah S, Anahory T, Déchaud H, Sarda P, Hédon B, Demaille J, Claustres M.
    Mol Hum Reprod; 2003 Feb; 9(2):111-6. PubMed ID: 12569181
    [Abstract] [Full Text] [Related]

  • 6. Molecular studies of loss of heterozygosity in retinoblastoma.
    Chiu LL, Lai PS, Low PS, Ling YL, Cheong PY, Chee CK, Wong PK, Lim AS.
    Ann Acad Med Singap; 1997 May; 26(3):315-9. PubMed ID: 9285025
    [Abstract] [Full Text] [Related]

  • 7. 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; 167(1):43-6. PubMed ID: 16682285
    [Abstract] [Full Text] [Related]

  • 8. 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; 42(1):65-72. PubMed ID: 16343894
    [Abstract] [Full Text] [Related]

  • 9. Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.
    Scheffer H, te Meerman GJ, Kruize YC, van den Berg AH, Penninga DP, Tan KE, der Kinderen DJ, Buys CH.
    Am J Hum Genet; 1989 Aug; 45(2):252-60. PubMed ID: 2569269
    [Abstract] [Full Text] [Related]

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

  • 11. Spectrum of RB1 mutations in argentine patients: 20-years experience in the molecular diagnosis of retinoblastoma.
    Ottaviani D, Parma D, Giliberto F, Ferrer M, Fandino A, Davila MT, Chantada G, Szijan I.
    Ophthalmic Genet; 2013 Dec; 34(4):189-98. PubMed ID: 23301675
    [Abstract] [Full Text] [Related]

  • 12. "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".
    Quiñonez-Silva G, Dávalos-Salas M, Recillas-Targa F, Ostrosky-Wegman P, Aranda DA, Benítez-Bribiesca L.
    Clin Epigenetics; 2016 Dec; 8():1. PubMed ID: 26753011
    [Abstract] [Full Text] [Related]

  • 13. Screening for RB1 mutations in tumor tissue using denaturing high performance liquid chromatography, multiplex ligation-dependent probe amplification, and loss of heterozygosity analysis.
    Sellner LN, Edkins E, Smith N.
    Pediatr Dev Pathol; 2006 Dec; 9(1):31-7. PubMed ID: 16808635
    [Abstract] [Full Text] [Related]

  • 14. The survival gene MED4 explains low penetrance retinoblastoma in patients with large RB1 deletion.
    Dehainault C, Garancher A, Castéra L, Cassoux N, Aerts I, Doz F, Desjardins L, Lumbroso L, Montes de Oca R, Almouzni G, Stoppa-Lyonnet D, Pouponnot C, Gauthier-Villars M, Houdayer C.
    Hum Mol Genet; 2014 Oct 01; 23(19):5243-50. PubMed ID: 24858910
    [Abstract] [Full Text] [Related]

  • 15. Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees.
    Munier FL, Wang MX, Spence MA, Thonney F, Balmer A, Pescia G, Donoso LA, Murphree AL.
    Arch Ophthalmol; 1993 Nov 01; 111(11):1507-11. PubMed ID: 8240106
    [Abstract] [Full Text] [Related]

  • 16. A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.
    Parsam VL, Kannabiran C, Honavar S, Vemuganti GK, Ali MJ.
    J Genet; 2009 Dec 01; 88(4):517-27. PubMed ID: 20090211
    [Abstract] [Full Text] [Related]

  • 17. Loss of heterozygosity and microsatellite instability at the retinoblastoma locus in osteosarcomas.
    Belchis DA, Meece CA, Benko FA, Rogan PK, Williams RA, Gocke CD.
    Diagn Mol Pathol; 1996 Sep 01; 5(3):214-9. PubMed ID: 8866236
    [Abstract] [Full Text] [Related]

  • 18. [Low-penetrance retinoblastoma due to exons 24 and 25 deletions in the Rb1 gene].
    Du C, Jiang Y, Gallie BL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct 01; 19(5):370-4. PubMed ID: 12362308
    [Abstract] [Full Text] [Related]

  • 19. Deletion of Rb1 gene in late osteosarcoma from survivor of unilateral retinoblastoma--a case report.
    Lee SY, Jeon DG, Lee JS, Hwang CS, Huh K, Lee TW, Hong SI.
    J Korean Med Sci; 1996 Feb 01; 11(1):94-8. PubMed ID: 8703379
    [Abstract] [Full Text] [Related]

  • 20. Molecular genetic considerations in osteosarcoma.
    Hansen MF.
    Clin Orthop Relat Res; 1991 Sep 01; (270):237-46. PubMed ID: 1679382
    [Abstract] [Full Text] [Related]

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