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Journal Abstract Search

89 related items for PubMed ID: 8100222

  • 1. Utilization of a polymorphic variable-number-tandem-repeat DNA region within the RB1 gene for early diagnosis of hereditary retinoblastoma.
    Herzog R, Ben Arush MW, Ezer S, On MG, Lev Z.
    Isr J Med Sci; 1993 May; 29(5):312-3. PubMed ID: 8100222
    [No Abstract] [Full Text] [Related]

  • 2. Molecular analysis of alleles segregation at RFLPs within RB-1 gene in four families with hereditary retinoblastoma.
    Kostyk E, Wieckiewicz J, Sutkowska A, Zygulska-Mach H, Pietrzyk JJ.
    Mater Med Pol; 1994 May; 26(3):105-8. PubMed ID: 7603079
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  • 3. Prediction of the risk of hereditary retinoblastoma, using DNA polymorphisms within the retinoblastoma gene.
    Wiggs J, Nordenskjöld M, Yandell D, Rapaport J, Grondin V, Janson M, Werelius B, Petersen R, Craft A, Riedel K.
    N Engl J Med; 1988 Jan 21; 318(3):151-7. PubMed ID: 2892131
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  • 4. [VNTR-PCR in diagnosis of inherited Rb gene mutation].
    Zajaczek S, Górski B, Débniak T, Podolski J, Lubiński J, Krzystolik Z, Iwanicka T, Sagan Z.
    Klin Oczna; 1994 Jan 21; 96(8-9):290-2. PubMed ID: 7897998
    [Abstract] [Full Text] [Related]

  • 5. Dde I RFLP may falsify linkage analysis of hereditary retinoblastoma when using SSCP of p88PR0.6 region.
    Sütterlin MW, Sleiman PA, Price E, Onadim Z, Delhanty J.
    Anticancer Res; 2000 Jan 21; 20(6D):5233-6. PubMed ID: 11326701
    [Abstract] [Full Text] [Related]

  • 6. [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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  • 8. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.
    Choy KW, Pang CP, Yu CB, Wong HL, Ng JS, Fan DS, Lo KW, Chai JT, Wang J, Fu W, Lam DS.
    Hum Mutat; 2002 Nov 30; 20(5):408. PubMed ID: 12402348
    [Abstract] [Full Text] [Related]

  • 9. Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient.
    Alonso J, Menéndez I, López A, Frayle H, Ruisánchez N, Pestaña A.
    Genes Chromosomes Cancer; 2004 Jul 30; 40(3):271-5. PubMed ID: 15139006
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  • 11. Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression.
    Albrecht P, Ansperger-Rescher B, Schüler A, Zeschnigk M, Gallie B, Lohmann DR.
    Hum Mutat; 2005 Nov 30; 26(5):437-45. PubMed ID: 16127685
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  • 13. The usefulness of three biallelic restriction fragment length polymorphisms versus a polymorphic dinucleotide tandem repeat polymorphism at the low-density-lipoprotein receptor gene locus for diagnosis of familial hypercholesterolemia.
    Weiss N, Gudnasson V, Ostwald P, Humphries S, Schuster H, Keller C.
    Dis Markers; 1997 Nov 30; 13(3):141-51. PubMed ID: 9405927
    [Abstract] [Full Text] [Related]

  • 14. [Retinoblastoma: clinical and molecular diagnostic aspects].
    Thonney F, Munier FL, Balmer A, Pescia G, Schorderet DF.
    Praxis (Bern 1994); 1996 Aug 27; 85(35):1058-62. PubMed ID: 8848678
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  • 16. Nonisotopic labelling of a variable number of tandem repeat probe by nick translation with biotinylated nucleotides.
    Rose M, Nagai T, Niemann C.
    Exp Clin Immunogenet; 1990 Aug 27; 7(3):200-2. PubMed ID: 1974450
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  • 19. Molecular studies of loss of heterozygosity in Chinese sporadic retinoblastoma patients.
    Zhang XL, Fu WL, Zhao HX, Zhou LX, Huang JF, Wang JH.
    Clin Chim Acta; 2005 Aug 27; 358(1-2):75-80. PubMed ID: 15921673
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