164 related articles for article (PubMed ID: 23414820)
21. 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]
22. Polymorphisms in the CAG repeat--a source of error in Huntington disease DNA testing.
Yu S; Fimmel A; Fung D; Trent RJ
Clin Genet; 2000 Dec; 58(6):469-72. PubMed ID: 11149616
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Huntington's disease: diagnosis by amplification of the CAG repeat.
Upton JD; Avery S; Parkin P; George PM
N Z Med J; 1995 Mar; 108(995):78-80. PubMed ID: 7891947
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. 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]
28. Triplet repeat primed PCR (TP PCR) in molecular diagnostic testing for Friedreich ataxia.
Ciotti P; Di Maria E; Bellone E; Ajmar F; Mandich P
J Mol Diagn; 2004 Nov; 6(4):285-9. PubMed ID: 15507666
[TBL] [Abstract][Full Text] [Related]
29. [Population and family studies of CAG repeats in the IT-15 gene].
Malysheva OV; Ivashchenko TE; Baranov VS
Genetika; 2001 Mar; 37(3):402-6. PubMed ID: 11357373
[TBL] [Abstract][Full Text] [Related]
30. Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease.
Nance MA; Mathias-Hagen V; Breningstall G; Wick MJ; McGlennen RC
Neurology; 1999 Jan; 52(2):392-4. PubMed ID: 9932964
[TBL] [Abstract][Full Text] [Related]
31. Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.
Veitch NJ; Ennis M; McAbney JP; ; Shelbourne PF; Monckton DG
DNA Repair (Amst); 2007 Jun; 6(6):789-96. PubMed ID: 17293170
[TBL] [Abstract][Full Text] [Related]
32. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standard.
Bruland O; Almqvist EW; Goldberg YP; Boman H; Hayden MR; Knappskog PM
Clin Genet; 1999 Mar; 55(3):198-202. PubMed ID: 10334474
[TBL] [Abstract][Full Text] [Related]
35. Exploring the correlates of intermediate CAG repeats in Huntington disease.
Ha AD; Jankovic J
Postgrad Med; 2011 Sep; 123(5):116-21. PubMed ID: 21904093
[TBL] [Abstract][Full Text] [Related]
36. DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.
Wang CK; Wu YR; Hwu WL; Chen CM; Ro LS; Chen ST; Gwinn-Hardy K; Yang CC; Wu RM; Chen TF; Wang HC; Chao MC; Chiu MJ; Lu CJ; Lee-Chen GJ
Eur Neurol; 2004; 52(2):96-100. PubMed ID: 15273431
[TBL] [Abstract][Full Text] [Related]
37. Detection of large expansions in myotonic dystrophy type 1 using triplet primed PCR.
Singh S; Zhang A; Dlouhy S; Bai S
Front Genet; 2014; 5():94. PubMed ID: 24795756
[TBL] [Abstract][Full Text] [Related]
38. Triplet Repeat Primed PCR (TP-PCR) in Molecular Diagnostic Testing for Spinocerebellar Ataxia Type 3 (SCA3).
Melo AR; Ramos A; Kazachkova N; Raposo M; Bettencourt BF; Rendeiro AR; Kay T; Vasconcelos J; Bruges-Armas J; Lima M
Mol Diagn Ther; 2016 Dec; 20(6):617-622. PubMed ID: 27647319
[TBL] [Abstract][Full Text] [Related]
39. A reproducible assay of polymerase chain reaction to detect trinucleotide repeat expansion of Huntington's disease and senile chorea.
Watanabe M; Abe K; Aoki M; Kameya T; Itoyama Y; Shoji M; Ikeda M; Iizuka T; Hirai S
Neurol Res; 1996 Feb; 18(1):16-8. PubMed ID: 8714530
[TBL] [Abstract][Full Text] [Related]
40. Two novel single-base-pair substitutions adjacent to the CAG repeat in the huntington disease gene (IT15): implications for diagnostic testing.
Margolis RL; Stine OC; Callahan C; Rosenblatt A; Abbott MH; Sherr M; Ross CA
Am J Hum Genet; 1999 Jan; 64(1):323-6. PubMed ID: 9915978
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
