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Journal Abstract Search

356 related items for PubMed ID: 16225399

  • 1. 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; 9(3):200-11. PubMed ID: 16225399
    [Abstract] [Full Text] [Related]

  • 2. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
    Amare Kadam PS, Ghule P, Jose J, Bamne M, Kurkure P, Banavali S, Sarin R, Advani S.
    Cancer Genet Cytogenet; 2004 Apr 01; 150(1):33-43. PubMed ID: 15041221
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  • 3. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Apr 01; 33(1):53-61. PubMed ID: 23715307
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  • 4. p53 gene gets altered by various mechanisms: studies in childhood sarcomas and retinoblastoma.
    Ghule P, Kadam PA, Jambhekar N, Bamne M, Pai S, Nair C, Banavali S, Puri A, Agarwal M.
    Med Sci Monit; 2006 Dec 01; 12(12):BR385-396. PubMed ID: 17136003
    [Abstract] [Full Text] [Related]

  • 5. RB1 germ-line deletions in Argentine retinoblastoma patients.
    Fernández C, Repetto K, Dalamon V, Bergonzi F, Ferreiro V, Szijan I.
    Mol Diagn Ther; 2007 Dec 01; 11(1):55-61. PubMed ID: 17286450
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  • 8. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
    Parma D, Ferrer M, Luce L, Giliberto F, Szijan I.
    PLoS One; 2017 Dec 01; 12(12):e0189736. PubMed ID: 29261756
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  • 10. 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 01; 7(7):1445-51. PubMed ID: 1352398
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  • 11. 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
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  • 12. 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 07; 51(3):208-14. PubMed ID: 24225018
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  • 13. Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.
    Shimizu T, Toguchida J, Kato MV, Kaneko A, Ishizaki K, Sasaki MS.
    Am J Hum Genet; 1994 May 07; 54(5):793-800. PubMed ID: 8178820
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  • 14. 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 07; 32A(10):1749-52. PubMed ID: 8983285
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  • 15. 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 07; 30(5):842-51. PubMed ID: 19280657
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  • 16. Spectrum of germline RB1 mutations and clinical manifestations in retinoblastoma patients from Thailand.
    Rojanaporn D, Boontawon T, Chareonsirisuthigul T, Thanapanpanich O, Attaseth T, Saengwimol D, Anurathapan U, Sujirakul T, Kaewkhaw R, Hongeng S.
    Mol Vis; 2018 May 07; 24():778-788. PubMed ID: 30636860
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  • 17. Two novel cases of trilateral retinoblastoma: genetics and review of the literature.
    D'Elia G, Grotta S, Del Bufalo F, De Ioris MA, Surace C, Sirleto P, Romanzo A, Cozza R, Locatelli F, Angioni A.
    Cancer Genet; 2013 Nov 07; 206(11):398-401. PubMed ID: 24412019
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  • 19. 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 07; 124():48-55. PubMed ID: 24810223
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