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Journal Abstract Search

181 related items for PubMed ID: 8983285

  • 1.
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  • 2. 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]

  • 3. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Sep 07; 33(1):53-61. PubMed ID: 23715307
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  • 4. Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.
    Cowell JK, Smith T, Bia B.
    Eur J Hum Genet; 1994 Sep 07; 2(4):281-90. PubMed ID: 7704558
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  • 5. [Genetics of retinoblastoma].
    Minoda K.
    Nihon Rinsho; 1995 Nov 07; 53(11):2774-8. PubMed ID: 8538043
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  • 7. 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 07; 61(2):282-94. PubMed ID: 9311732
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  • 11. 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 07; 7(7):1445-51. PubMed ID: 1352398
    [Abstract] [Full Text] [Related]

  • 12. Exon-by-exon screening for RB germline mutations using Heteroduplex-SSCP analysis.
    Zhang Q, Minoda K, Zeng R, Wu Z, Xiao X, Li S, Zhang F.
    Yan Ke Xue Bao; 1997 Mar 07; 13(1):5-11. PubMed ID: 11189328
    [Abstract] [Full Text] [Related]

  • 13. Mutation detection and genetic counseling in retinoblastoma using heteroduplex analysis.
    Zhang Q, Minoda K.
    Jpn J Ophthalmol; 1995 Mar 07; 39(4):432-7. PubMed ID: 8926652
    [Abstract] [Full Text] [Related]

  • 14. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
    Parma D, Ferrer M, Luce L, Giliberto F, Szijan I.
    PLoS One; 2017 Mar 07; 12(12):e0189736. PubMed ID: 29261756
    [Abstract] [Full Text] [Related]

  • 15. 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 07; 11(1):55-61. PubMed ID: 17286450
    [Abstract] [Full Text] [Related]

  • 16. The RB1 gene mutation in a child with ectopic intracranial retinoblastoma.
    Onadim Z, Woolford AJ, Kingston JE, Hungerford JL.
    Br J Cancer; 1997 Mar 07; 76(11):1405-9. PubMed ID: 9400934
    [Abstract] [Full Text] [Related]

  • 17. Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan.
    Yousef YA, Tbakhi A, Al-Hussaini M, AlNawaiseh I, Saab A, Afifi A, Naji M, Mohammad M, Deebajah R, Jaradat I, Sultan I, Mehyar M.
    Fam Cancer; 2018 Apr 07; 17(2):261-268. PubMed ID: 28803391
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Detection of RB germline mutations using exon-by-exon heteroduplex analysis compared with SSCP.
    Zhang Q, Minoda K.
    Yan Ke Xue Bao; 1996 Sep 07; 12(3):151-7. PubMed ID: 9639842
    [Abstract] [Full Text] [Related]

  • 20. Spectrum of germline mutations in RB1 in Chinese patients with retinoblastoma: Application of targeted next-generation sequencing.
    Zou Y, Li J, Hua P, Liang T, Ji X, Zhao P.
    Mol Vis; 2021 Sep 07; 27():1-16. PubMed ID: 33456302
    [Abstract] [Full Text] [Related]

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