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Journal Abstract Search

259 related items for PubMed ID: 22084214

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  • 6. Role of genetic testing in retinoblastoma management at a tertiary referral centre.
    Pradhan MA, Ng Y, Strickland A, George PM, Raizis A, Warrington J, Vincent AL.
    Clin Exp Ophthalmol; 2010 Apr; 38(3):231-6. PubMed ID: 20447117
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  • 9. Genotype-phenotype correlation in the presentation of retinoblastoma among 149 patients.
    Frenkel S, Zloto O, Sagi M, Fraenkel A, Pe'er J.
    Exp Eye Res; 2016 May; 146():313-317. PubMed ID: 27068507
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  • 14. 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; 41(5):735-40. PubMed ID: 15763650
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  • 16. [From gene to disease; retinoblastoma and the RB1 gene].
    Scheffer H, Imhof SM, Moll AC.
    Ned Tijdschr Geneeskd; 2001 Jun 30; 145(26):1245-7. PubMed ID: 11455690
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  • 17. Clinical findings and molecular diagnosis of retinoblastoma in older children.
    Sheck LH, Ng YS, Watson M, Vincent AL.
    Ophthalmic Genet; 2013 Dec 30; 34(4):238-42. PubMed ID: 23289805
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  • 18. Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening.
    Harbour JW.
    Ophthalmology; 1998 Aug 30; 105(8):1442-7. PubMed ID: 9709755
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  • 20. 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 Aug 30; 9(1):31-7. PubMed ID: 16808635
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