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3. 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]
4. Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease. Ranen NG; Stine OC; Abbott MH; Sherr M; Codori AM; Franz ML; Chao NI; Chung AS; Pleasant N; Callahan C Am J Hum Genet; 1995 Sep; 57(3):593-602. PubMed ID: 7668287 [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. Trinucleotide repeat length and progression of illness in Huntington's disease. Kieburtz K; MacDonald M; Shih C; Feigin A; Steinberg K; Bordwell K; Zimmerman C; Srinidhi J; Sotack J; Gusella J J Med Genet; 1994 Nov; 31(11):872-4. PubMed ID: 7853373 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset. Trottier Y; Biancalana V; Mandel JL J Med Genet; 1994 May; 31(5):377-82. PubMed ID: 8064815 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis]. Sánchez A; Milà M; Castellví-Bel S; Calopa M; Genís D; Jiménez D; Estivill X Med Clin (Barc); 1997 May; 108(18):687-90. PubMed ID: 9324583 [TBL] [Abstract][Full Text] [Related]
11. Molecular analysis of late onset Huntington's disease. Kremer B; Squitieri F; Telenius H; Andrew SE; Theilmann J; Spence N; Goldberg YP; Hayden MR J Med Genet; 1993 Dec; 30(12):991-5. PubMed ID: 8133510 [TBL] [Abstract][Full Text] [Related]
12. [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]
13. 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]
14. A study of the Huntington's disease associated trinucleotide repeat in the Scottish population. Barron LH; Warner JP; Porteous M; Holloway S; Simpson S; Davidson R; Brock DJ J Med Genet; 1993 Dec; 30(12):1003-7. PubMed ID: 8133495 [TBL] [Abstract][Full Text] [Related]
15. Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15. Stine OC; Pleasant N; Franz ML; Abbott MH; Folstein SE; Ross CA Hum Mol Genet; 1993 Oct; 2(10):1547-9. PubMed ID: 8268907 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Huntington's disease--advances in gene mapping]. Nakamura S Nihon Rinsho; 1993 Sep; 51(9):2481-7. PubMed ID: 8411732 [TBL] [Abstract][Full Text] [Related]
18. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms. Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771 [TBL] [Abstract][Full Text] [Related]
19. A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes. Warner JP; Barron LH; Brock DJ Mol Cell Probes; 1993 Jun; 7(3):235-9. PubMed ID: 8366869 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]