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.
121 related articles for article (PubMed ID: 19378429)
1. Use of capillary electrophoresis for accurate determination of CAG repeats causing Huntington disease. An oligonucleotide design avoiding shadow bands. Blanco S; Suarez A; Gandia-Pla S; Gómez-Llorente C; Antúnez A; Gómez-Capilla JA; Fárez-Vidal ME Scand J Clin Lab Invest; 2008; 68(7):577-84. PubMed ID: 19378429 [TBL] [Abstract][Full Text] [Related]
2. A novel PCR-based approach for the detection of the Huntington disease associated trinucleotide repeat expansion. Panagopoulos I; Lassen C; Kristoffersson U; Aman P Hum Mutat; 1999; 13(3):232-6. PubMed ID: 10090478 [TBL] [Abstract][Full Text] [Related]
3. Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards. Williams LC; Hegde MR; Herrera G; Stapleton PM; Love DR Mol Cell Probes; 1999 Aug; 13(4):283-9. PubMed ID: 10441201 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay. Zhao M; Lee CG; Law HY; Chong SS Neurodegener Dis; 2016; 16(5-6):348-51. PubMed ID: 27207688 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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; 20(3):233. PubMed ID: 12204002 [TBL] [Abstract][Full Text] [Related]
8. 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]
10. 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; 66(3):281-6. PubMed ID: 8985488 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Advances in Huntington's disease diagnostics: development of a standard reference material. Levin BC; Richie KL; Jakupciak JP Expert Rev Mol Diagn; 2006 Jul; 6(4):587-96. PubMed ID: 16824032 [TBL] [Abstract][Full Text] [Related]
14. [Molecular diagnosis of Huntington's disease: an analysis of two large families]. Zeng Y; Chen M; Mao Y Zhonghua Yi Xue Za Zhi; 1995 Nov; 75(11):689-93, 711-2. PubMed ID: 8697093 [TBL] [Abstract][Full Text] [Related]
15. [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 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Triplet repeat primed PCR simplifies testing for Huntington disease. Jama M; Millson A; Miller CE; Lyon E J Mol Diagn; 2013 Mar; 15(2):255-62. PubMed ID: 23414820 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. The repeat expansion detection method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitations. Martorell L; Pujana MA; Volpini V; Sanchez A; Joven J; Vilella E; Estivill X Hum Mutat; 1997; 10(6):486-8. PubMed ID: 9401013 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]