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.
2. 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]
3. A Novel Triplet-Primed PCR Assay to Detect the Full Range of Trinucleotide CAG Repeats in the Huntingtin Gene ( De Luca A; Morella A; Consoli F; Fanelli S; Thibert JR; Statt S; Latham GJ; Squitieri F Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33567536 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Simple procedure for automatic detection of unstable alleles in the myotonic dystrophy and Huntington's disease loci. Falk M; Vojtísková M; Lukás Z; Kroupová I; Froster U Genet Test; 2006; 10(2):85-97. PubMed ID: 16792511 [TBL] [Abstract][Full Text] [Related]
7. 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. Single-step scalable-throughput molecular screening for Huntington disease. Teo CR; Wang W; Yang Law H; Lee CG; Chong SS Clin Chem; 2008 Jun; 54(6):964-72. PubMed ID: 18403567 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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; 58(1):28-30. PubMed ID: 25464109 [TBL] [Abstract][Full Text] [Related]
11. Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping. Zhao M; Cheah FSH; Tan ASC; Lian M; Phang GP; Agarwal A; Chong SS Sci Rep; 2019 Nov; 9(1):16481. PubMed ID: 31712634 [TBL] [Abstract][Full Text] [Related]
12. Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout. Magri S; Nanetti L; Mongelli A; Rizzo E; Taroni F; Mariotti C; Gellera C Am J Med Genet A; 2021 Feb; 185(2):397-400. PubMed ID: 33247537 [TBL] [Abstract][Full Text] [Related]
13. [Genetic diagnosis of Huntington disease]. Mo YQ; Li LY; Lu GX Yi Chuan; 2005 Nov; 27(6):861-4. PubMed ID: 16378928 [TBL] [Abstract][Full Text] [Related]
14. [Methods of determination of the number of CTG/CAG repeats in trinucleotide repeats in the human genome]. Falk M; Froster U; Vojtísková M Cas Lek Cesk; 2003; 142(10):609-14. PubMed ID: 14635426 [TBL] [Abstract][Full Text] [Related]
15. Nonisotopic method for accurate detection of (CAG)n repeats causing Huntington disease. Muglia M; Leone O; Annesi G; Gabriele AL; Imbrogno E; Grandinetti C; Conforti FL; Naso F; Brancati C Clin Chem; 1996 Oct; 42(10):1601-3. PubMed ID: 8855141 [TBL] [Abstract][Full Text] [Related]
16. An intergenerational contraction of a fully penetrant Huntington disease allele to a reduced penetrance allele: interpretation of results and significance for risk assessment and genetic counseling. Nahhas F; Garbern J; Feely S; Feldman GL Am J Med Genet A; 2009 Feb; 149A(4):732-6. PubMed ID: 19267413 [TBL] [Abstract][Full Text] [Related]
17. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington's disease. Aziz NA; van Belzen MJ; Coops ID; Belfroid RD; Roos RA Eur J Med Genet; 2011; 54(4):e413-8. PubMed ID: 21540131 [TBL] [Abstract][Full Text] [Related]
18. Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach. Mariani LL; Tesson C; Charles P; Cazeneuve C; Hahn V; Youssov K; Freeman L; Grabli D; Roze E; Noël S; Peuvion JN; Bachoud-Levi AC; Brice A; Stevanin G; Durr A JAMA Neurol; 2016 Sep; 73(9):1105-14. PubMed ID: 27400454 [TBL] [Abstract][Full Text] [Related]
19. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. Ciosi M; Maxwell A; Cumming SA; Hensman Moss DJ; Alshammari AM; Flower MD; Durr A; Leavitt BR; Roos RAC; ; ; Holmans P; Jones L; Langbehn DR; Kwak S; Tabrizi SJ; Monckton DG EBioMedicine; 2019 Oct; 48():568-580. PubMed ID: 31607598 [TBL] [Abstract][Full Text] [Related]
20. Analysis of short tandem repeat markers by capillary array electrophoresis. Mansfield ES; Wilson RB; Fortina P Methods Mol Biol; 2001; 163():151-61. PubMed ID: 11242940 [No Abstract] [Full Text] [Related] [Next] [New Search]