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4. Mutation analysis in patients with possible but apparently sporadic Huntington's disease. Davis MB; Bateman D; Quinn NP; Marsden CD; Harding AE Lancet; 1994 Sep; 344(8924):714-7. PubMed ID: 7915776 [TBL] [Abstract][Full Text] [Related]
5. 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; 92(2):132-4. PubMed ID: 7484060 [TBL] [Abstract][Full Text] [Related]
6. Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability. Williams LC; Hegde MR; Nagappan R; Faull RL; Giles J; Winship I; Snow K; Love DR Genet Test; 2000; 4(1):55-60. PubMed ID: 10794362 [TBL] [Abstract][Full Text] [Related]
8. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing. Andrew SE; Goldberg YP; Theilmann J; Zeisler J; Hayden MR Hum Mol Genet; 1994 Jan; 3(1):65-7. PubMed ID: 8162053 [TBL] [Abstract][Full Text] [Related]
9. Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene. Zühlke C; Riess O; Bockel B; Lange H; Thies U Hum Mol Genet; 1993 Dec; 2(12):2063-7. PubMed ID: 8111374 [TBL] [Abstract][Full Text] [Related]
10. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range. De Rooij KE; De Koning Gans PA; Skraastad MI; Belfroid RD; Vegter-Van Der Vlis M; Roos RA; Bakker E; Van Ommen GJ; Den Dunnen JT; Losekoot M J Med Genet; 1993 Dec; 30(12):996-1002. PubMed ID: 8133511 [TBL] [Abstract][Full Text] [Related]
11. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Andrew SE; Goldberg YP; Kremer B; Telenius H; Theilmann J; Adam S; Starr E; Squitieri F; Lin B; Kalchman MA Nat Genet; 1993 Aug; 4(4):398-403. PubMed ID: 8401589 [TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease. Mandich P; Di Maria E; Bellone E; Ajmar F; Abbruzzese G Eur Neurol; 1996; 36(6):348-52. PubMed ID: 8954302 [TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent. Telenius H; Kremer HP; Theilmann J; Andrew SE; Almqvist E; Anvret M; Greenberg C; Greenberg J; Lucotte G; Squitieri F Hum Mol Genet; 1993 Oct; 2(10):1535-40. PubMed ID: 8268906 [TBL] [Abstract][Full Text] [Related]
16. Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea. MacMillan JC; Morrison PJ; Nevin NC; Shaw DJ; Harper PS; Quarrell OW; Snell RG J Med Genet; 1993 Dec; 30(12):1012-3. PubMed ID: 8133497 [TBL] [Abstract][Full Text] [Related]
17. De novo expansion of a (CAG)n repeat in sporadic Huntington's disease. Myers RH; MacDonald ME; Koroshetz WJ; Duyao MP; Ambrose CM; Taylor SA; Barnes G; Srinidhi J; Lin CS; Whaley WL Nat Genet; 1993 Oct; 5(2):168-73. PubMed ID: 8252042 [TBL] [Abstract][Full Text] [Related]
18. Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes. Kremer B; Almqvist E; Theilmann J; Spence N; Telenius H; Goldberg YP; Hayden MR Am J Hum Genet; 1995 Aug; 57(2):343-50. PubMed ID: 7668260 [TBL] [Abstract][Full Text] [Related]
19. A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats. Kremer B; Goldberg P; Andrew SE; Theilmann J; Telenius H; Zeisler J; Squitieri F; Lin B; Bassett A; Almqvist E N Engl J Med; 1994 May; 330(20):1401-6. PubMed ID: 8159192 [TBL] [Abstract][Full Text] [Related]
20. Recombination of 4p16 DNA markers in an unusual family with Huntington disease. Pritchard C; Zhu N; Zuo J; Bull L; Pericak-Vance MA; Vance JM; Roses AD; Milatovich A; Francke U; Cox DR Am J Hum Genet; 1992 Jun; 50(6):1218-30. PubMed ID: 1350884 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]