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Journal Abstract Search

554 related items for PubMed ID: 23715307

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

  • 2. 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; 25(3):166-73. PubMed ID: 11480772
    [Abstract] [Full Text] [Related]

  • 3. 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]

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

  • 5. 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]

  • 6. Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.
    Alonso J, Frayle H, Menéndez I, López A, García-Miguel P, Abelairas J, Sarret E, Vendrell MT, Navajas A, Artigas M, Indiano JM, Carbone A, Torrenteras C, Palacios I, Pestaña A.
    Hum Mutat; 2005 Jan; 25(1):99. PubMed ID: 15605413
    [Abstract] [Full Text] [Related]

  • 7. Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India.
    Bamne MN, Ghule PN, Jose J, Banavali SD, Kurkure PA, Amare Kadam PS.
    Genet Test; 2005 Jan; 9(3):200-11. PubMed ID: 16225399
    [Abstract] [Full Text] [Related]

  • 8. Genetic testing in Tunisian families with heritable retinoblastoma using a low cost approach permits accurate risk prediction in relatives and reveals incomplete penetrance in adults.
    Ayari Jeridi H, Bouguila H, Ansperger-Rescher B, Baroudi O, Mdimegh I, Omran I, Charradi K, Bouzayene H, Benammar-Elgaaïed A, Lohmann DR.
    Exp Eye Res; 2014 Jul; 124():48-55. PubMed ID: 24810223
    [Abstract] [Full Text] [Related]

  • 9. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.
    Hogg A, Onadim Z, Baird PN, Cowell JK.
    Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398
    [Abstract] [Full Text] [Related]

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

  • 11. 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]

  • 12. 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; 91(8):379-84. PubMed ID: 27021801
    [Abstract] [Full Text] [Related]

  • 13. Independent constitutional germline mutations occurring in the RB1 gene in cousins with bilateral retinoblastoma.
    Bia B, Cowell JK.
    Oncogene; 1995 Sep 07; 11(5):977-9. PubMed ID: 7675457
    [Abstract] [Full Text] [Related]

  • 14. Rapid identification of germline mutations in retinoblastoma by protein truncation testing.
    Tsai T, Fulton L, Smith BJ, Mueller RL, Gonzalez GA, Uusitalo MS, O'Brien JM.
    Arch Ophthalmol; 2004 Feb 07; 122(2):239-48. PubMed ID: 14769601
    [Abstract] [Full Text] [Related]

  • 15. [Genetics of retinoblastoma].
    Minoda K.
    Nihon Rinsho; 1995 Nov 07; 53(11):2774-8. PubMed ID: 8538043
    [Abstract] [Full Text] [Related]

  • 16. 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 07; 25(6):566-74. PubMed ID: 15884040
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Spectrum of RB1 mutations identified in 403 retinoblastoma patients.
    Price EA, Price K, Kolkiewicz K, Hack S, Reddy MA, Hungerford JL, Kingston JE, Onadim Z.
    J Med Genet; 2014 Mar 27; 51(3):208-14. PubMed ID: 24225018
    [Abstract] [Full Text] [Related]

  • 19. 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 27; 208(5):400-3. PubMed ID: 8766064
    [Abstract] [Full Text] [Related]

  • 20. 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]

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