These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
172 related articles for article (PubMed ID: 7480359)
21. Trinucleotide repeat elongation in the huntingtin gene in Huntington's disease patients from 85 French families. The French HD Research Group. Lucotte G; Aouizérate A; Loreille O; Gérard N; Turpin JC Genet Couns; 1994; 5(4):321-8. PubMed ID: 7888133 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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 [TBL] [Abstract][Full Text] [Related]
24. Trinucleotide repeat length and rate of progression of Huntington's disease. Illarioshkin SN; Igarashi S; Onodera O; Markova ED; Nikolskaya NN; Tanaka H; Chabrashwili TZ; Insarova NG; Endo K; Ivanova-Smolenskaya IA Ann Neurol; 1994 Oct; 36(4):630-5. PubMed ID: 7944295 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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; 69(5):653-62. PubMed ID: 9299885 [TBL] [Abstract][Full Text] [Related]
27. DNA analysis of Huntington's disease in southern Chinese. Chan V; Yu YL; Chan TP; Yip B; Chang CM; Wong MT; Chan YW; Chan TK J Med Genet; 1995 Feb; 32(2):120-4. PubMed ID: 7760321 [TBL] [Abstract][Full Text] [Related]
28. [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; 126(3-4):77-82. PubMed ID: 9863360 [TBL] [Abstract][Full Text] [Related]
29. Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes. Pêcheux C; Mouret JF; Dürr A; Agid Y; Feingold J; Brice A; Dodé C; Kaplan JC J Med Genet; 1995 May; 32(5):399-400. PubMed ID: 7616551 [TBL] [Abstract][Full Text] [Related]
30. A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population. Barron LH; Rae A; Holloway S; Brock DJ; Warner JP Hum Mol Genet; 1994 Jan; 3(1):173-5. PubMed ID: 8162020 [TBL] [Abstract][Full Text] [Related]
31. Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeat. Persichetti F; Ambrose CM; Ge P; McNeil SM; Srinidhi J; Anderson MA; Jenkins B; Barnes GT; Duyao MP; Kanaley L Mol Med; 1995 May; 1(4):374-83. PubMed ID: 8521295 [TBL] [Abstract][Full Text] [Related]
32. Molecular analysis of the Huntington's disease gene in New Zealand. Whitefield JE; Williams L; Snow K; Dixon J; Winship I; Stapleton PM; Faull RM; Love DR N Z Med J; 1996 Feb; 109(1015):27-30. PubMed ID: 8606810 [TBL] [Abstract][Full Text] [Related]
33. Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases. Goldberg YP; Andrew SE; Theilmann J; Kremer B; Squitieri F; Telenius H; Brown JD; Hayden MR J Med Genet; 1993 Dec; 30(12):987-90. PubMed ID: 8133509 [TBL] [Abstract][Full Text] [Related]
34. Limited expansion of the (CAG)n repeat of the Huntington gene: a premutation (?). Legius E; Cuppens H; Dierick H; Van Zandt K; Dom R; Fryns JP; Evers-Kiebooms G; Decruyenaere M; Demyttenaere K; Marynen P Eur J Hum Genet; 1994; 2(1):44-50. PubMed ID: 8044653 [TBL] [Abstract][Full Text] [Related]
36. Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease. Benitez J; Fernandez E; Garcia Ruiz P; Robledo M; Ramos C; Yébenes J Hum Genet; 1994 Nov; 94(5):563-4. PubMed ID: 7959696 [TBL] [Abstract][Full Text] [Related]
37. Analysis of the (CAG)n repeat causing Huntington's disease in a Mexican population. Alonso ME; Yescas P; Cisneros B; Martínez C; Silva G; Ochoa A; Montañez C Clin Genet; 1997 Apr; 51(4):225-30. PubMed ID: 9184242 [TBL] [Abstract][Full Text] [Related]
38. Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families. Nørremølle A; Riess O; Epplen JT; Fenger K; Hasholt L; Sørensen SA Hum Mol Genet; 1993 Sep; 2(9):1475-6. PubMed ID: 8242074 [TBL] [Abstract][Full Text] [Related]
39. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Cell; 1993 Mar; 72(6):971-83. PubMed ID: 8458085 [TBL] [Abstract][Full Text] [Related]
40. Analysis of the 5' upstream sequence of the Huntington's disease (HD) gene shows six new rare alleles which are unrelated to the age at onset of HD. Coles R; Leggo J; Rubinsztein DC J Med Genet; 1997 May; 34(5):371-4. PubMed ID: 9152833 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]