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Journal Abstract Search

412 related items for PubMed ID: 1352398

  • 1. 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
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  • 2. 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
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  • 3. A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 gene.
    Cowell JK, Bia B, Akoulitchev A.
    Oncogene; 1996 Jan 18; 12(2):431-6. PubMed ID: 8570221
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  • 4. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 18; 56(3):105-52. PubMed ID: 19728970
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  • 6. [Genetics of retinoblastoma].
    Minoda K.
    Nihon Rinsho; 1995 Nov 18; 53(11):2774-8. PubMed ID: 8538043
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  • 7. 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]

  • 8. 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 07; 25(3):166-73. PubMed ID: 11480772
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  • 9. [Diagnosis of a predisposition of retinoblastoma at the DNA level].
    Murakami Y.
    Gan To Kagaku Ryoho; 1991 Jan 07; 18(1):44-50. PubMed ID: 1670986
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  • 10. Molecular analysis of unknown beta-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with beta-thalassemias and beta-globin variants.
    Chinchang W, Viprakasit V, Pung-Amritt P, Tanphaichitr VS, Yenchitsomanus PT.
    Clin Biochem; 2005 Nov 07; 38(11):987-96. PubMed ID: 16139831
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  • 16. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Nov 07; 33(1):53-61. PubMed ID: 23715307
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  • 17. A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm.
    Weir-Thompson E, Condie A, Leonard RC, Prosser J.
    Oncogene; 1991 Dec 07; 6(12):2353-6. PubMed ID: 1662795
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  • 18. Retinoblastoma gene mutation in primary human renal cell carcinoma.
    Shuin T, Torigoe S, Kubota Y, Kishida T, Hosaka M, Horikoshi T, Yao M, Kondo K, Sakai N, Danenberg K.
    Oncol Res; 1995 Dec 07; 7(2):63-6. PubMed ID: 7579728
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  • 19. BRCA1 mutation screening using restriction endonuclease fingerprinting-single-strand conformation polymorphism in an automated capillary electrophoresis system.
    Kringen P, Egedal S, Pedersen JC, Harbitz TB, Tveit KM, Berg K, Børresen-Dale AL, Andersen TI.
    Electrophoresis; 2002 Dec 07; 23(24):4085-91. PubMed ID: 12481264
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  • 20. [The status of p53 gene in the primary retinoblastoma].
    Huang Q.
    Zhonghua Yan Ke Za Zhi; 1999 Jul 07; 35(4):248-51. PubMed ID: 11835813
    [Abstract] [Full Text] [Related]

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