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Journal Abstract Search

438 related items for PubMed ID: 16965319

  • 1. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles.
    Semaka A, Creighton S, Warby S, Hayden MR.
    Clin Genet; 2006 Oct; 70(4):283-94. PubMed ID: 16965319
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  • 2. Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.
    Goldberg YP, Kremer B, Andrew SE, Theilmann J, Graham RK, Squitieri F, Telenius H, Adam S, Sajoo A, Starr E.
    Nat Genet; 1993 Oct; 5(2):174-9. PubMed ID: 8252043
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  • 5. Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.
    Veitch NJ, Ennis M, McAbney JP, US-Venezuela Collaborative Research Project, Shelbourne PF, Monckton DG.
    DNA Repair (Amst); 2007 Jun 01; 6(6):789-96. PubMed ID: 17293170
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  • 8. Advances in Huntington's disease diagnostics: development of a standard reference material.
    Levin BC, Richie KL, Jakupciak JP.
    Expert Rev Mol Diagn; 2006 Jul 01; 6(4):587-96. PubMed ID: 16824032
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  • 9. Analysis of the (CAG)n repeat at the IT15 locus in a population from Calabria (southern Italy).
    Leone O, Muglia M, Gabriele AL, Annesi G, Conforti FL, Imbrogno E, Imbrogno L, Brancati C.
    Hum Biol; 1997 Oct 01; 69(5):653-62. PubMed ID: 9299885
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  • 10. [Molecular genetics of Huntington's disease].
    Goto J, Masuda N, Watanabe M, Kanazawa I.
    Rinsho Shinkeigaku; 1995 Dec 01; 35(12):1529-31. PubMed ID: 8752453
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  • 11. 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 01; 75(3):244-50. PubMed ID: 19250382
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  • 12. Polymorphic CAG repeat length in the androgen receptor gene and association with neurodegeneration in a heterozygous female carrier of Kennedy's disease.
    Greenland KJ, Beilin J, Castro J, Varghese PN, Zajac JD.
    J Neurol; 2004 Jan 01; 251(1):35-41. PubMed ID: 14999487
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  • 13. A new mutation for Huntington disease following maternal transmission of an intermediate allele.
    Semaka A, Kay C, Belfroid RD, Bijlsma EK, Losekoot M, van Langen IM, van Maarle MC, Oosterloo M, Hayden MR, van Belzen MJ.
    Eur J Med Genet; 2015 Jan 01; 58(1):28-30. PubMed ID: 25464109
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  • 15. Expansion of a (CAG)n repeat region in a sporadic case of HD.
    Bozza A, Malagù S, Calzolari E, Novelletto A, Pavoni M, del Senno L.
    Acta Neurol Scand; 1995 Aug 01; 92(2):132-4. PubMed ID: 7484060
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  • 16. Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
    Agostinho Lde A, Rocha CF, Medina-Acosta E, Barboza HN, da Silva AF, Pereira SP, da Silva Idos S, Paradela ER, Figueiredo AL, Nogueira Ede M, Alvarenga RM, Hernan Cabello P, dos Santos SR, Paiva CL.
    J Hum Genet; 2012 Dec 01; 57(12):796-803. PubMed ID: 23051704
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  • 19. [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 01; 32(1):103-9. PubMed ID: 8647411
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