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Journal Abstract Search

610 related items for PubMed ID: 8752453

  • 1. [Molecular genetics of Huntington's disease].
    Goto J, Masuda N, Watanabe M, Kanazawa I.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1529-31. PubMed ID: 8752453
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  • 2. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.
    Masuda N, Goto J, Murayama N, Watanabe M, Kondo I, Kanazawa I.
    J Med Genet; 1995 Sep; 32(9):701-5. PubMed ID: 8544189
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  • 3. Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.
    Dodé C, Dürr A, Pêcheux C, Mouret JF, Belal S, Bachner L, Agid Y, Kaplan JC, Brice A, Feingold J.
    C R Acad Sci III; 1993 Nov; 316(11):1374-80. PubMed ID: 8087617
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  • 4. DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.
    Wang CK, Wu YR, Hwu WL, Chen CM, Ro LS, Chen ST, Gwinn-Hardy K, Yang CC, Wu RM, Chen TF, Wang HC, Chao MC, Chiu MJ, Lu CJ, Lee-Chen GJ.
    Eur Neurol; 2004 Nov; 52(2):96-100. PubMed ID: 15273431
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  • 5. [Huntington's chorea: clinical aspects, genetics and current diagnosis].
    Spiegel R.
    Ther Umsch; 1995 Dec; 52(12):814-20. PubMed ID: 8539653
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  • 6. Trinucleotide repeat length instability and age of onset in Huntington's disease.
    Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, Folstein S, Ross C, Franz M, Abbott M.
    Nat Genet; 1993 Aug; 4(4):387-92. PubMed ID: 8401587
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  • 10. 4p16.3 haplotype modifying age at onset of Huntington disease.
    Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen JE, Sørensen SA, Hasholt L.
    Clin Genet; 2009 Mar; 75(3):244-50. PubMed ID: 19250382
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  • 11. Molecular detection of new mutations, resolution of ambiguous results and complex genetic counseling issues in Huntington disease.
    Alford RL, Ashizawa T, Jankovic J, Caskey CT, Richards CS.
    Am J Med Genet; 1996 Dec 18; 66(3):281-6. PubMed ID: 8985488
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  • 13. [Importance of the number of trinucleotide repeat expansions in the clinical manifestations of Huntington's chorea].
    Vojvodić N, Culjković B, Romac S, Stojković O, Sternić N, Sokić D, Kostić VS.
    Srp Arh Celok Lek; 1998 Dec 18; 126(3-4):77-82. PubMed ID: 9863360
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  • 14. Genetic background of Huntington disease in Croatia: Molecular analysis of CAG, CCG, and Delta2642 (E2642del) polymorphisms.
    Hećimović S, Klepac N, Vlasić J, Vojta A, Janko D, Skarpa-Prpić I, Canki-Klain N, Marković D, Bozikov J, Relja M, Pavelić K.
    Hum Mutat; 2002 Sep 18; 20(3):233. PubMed ID: 12204002
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  • 15. Advances in Huntington's disease diagnostics: development of a standard reference material.
    Levin BC, Richie KL, Jakupciak JP.
    Expert Rev Mol Diagn; 2006 Jul 18; 6(4):587-96. PubMed ID: 16824032
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  • 18. [Huntington's disease: clinical and molecular genetics].
    Warita H, Shiro Y, Kashihara K, Abe K.
    Nihon Rinsho; 1999 Apr 18; 57(4):896-9. PubMed ID: 10222786
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  • 19. Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.
    Yapijakis C, Vassilopoulos D, Tzagournisakis M, Maris T, Fesdjian C, Papageorgiou C, Plaitakis A.
    Eur J Hum Genet; 1995 Apr 18; 3(4):228-34. PubMed ID: 8528671
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  • 20. [Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects].
    Illarioshkin SN, Ivanova-Smolenskaia IA, Markova ED, Nikol'skaia NN, Chabrashvili TZ, Insarova NG.
    Genetika; 1996 Jan 18; 32(1):103-9. PubMed ID: 8647411
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