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4. A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene. Baxendale S; MacDonald ME; Mott R; Francis F; Lin C; Kirby SF; James M; Zehetner G; Hummerich H; Valdes J Nat Genet; 1993 Jun; 4(2):181-6. PubMed ID: 8348156 [TBL] [Abstract][Full Text] [Related]
5. Trinucleotide repeat expansion and human disease. Hummerich H; Lehrach H Electrophoresis; 1995 Sep; 16(9):1698-704. PubMed ID: 8582359 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genes with triplet repeats: a new class of mutations causing neurological diseases. Plassart E; Fontaine B Biomed Pharmacother; 1994; 48(5-6):191-7. PubMed ID: 7999979 [TBL] [Abstract][Full Text] [Related]
8. Trinucleotide repeats in neurologic diseases: an hypothesis concerning the pathogenesis of Huntington's disease, Kennedy's disease, and spinocerebellar ataxia type I. Cha JH; Dure LS Life Sci; 1994; 54(20):1459-64. PubMed ID: 8190020 [TBL] [Abstract][Full Text] [Related]
9. Unstable triplet repeat sequences: a source of cancer mutations? Panzer S; Kuhl DP; Caskey CT Stem Cells; 1995 Mar; 13(2):146-57. PubMed ID: 7787780 [TBL] [Abstract][Full Text] [Related]
10. Trinucleotide repeat expansion in neurological disease. La Spada AR; Paulson HL; Fischbeck KH Ann Neurol; 1994 Dec; 36(6):814-22. PubMed ID: 7998766 [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. Trinucleotide repeat disorders in humans: discussions of mechanisms and medical issues. Timchenko LT; Caskey CT FASEB J; 1996 Dec; 10(14):1589-97. PubMed ID: 9002550 [TBL] [Abstract][Full Text] [Related]
13. No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3. Hellenbroich Y; Kaulich M; Opitz S; Schwinger E; Zühlke C Psychiatr Genet; 2004 Jun; 14(2):61-3. PubMed ID: 15167689 [TBL] [Abstract][Full Text] [Related]
14. A single trinucleotide, 5'AGC3'/5'GCT3', of the triplet-repeat disease genes confers metal ion-induced non-B DNA structure. Kohwi Y; Wang H; Kohwi-Shigematsu T Nucleic Acids Res; 1993 Dec; 21(24):5651-5. PubMed ID: 8284211 [TBL] [Abstract][Full Text] [Related]
15. Unstable trinucleotide repeats and the diagnosis of neurodegenerative disease. Orr HT Hum Pathol; 1994 Jun; 25(6):598-601. PubMed ID: 8013951 [TBL] [Abstract][Full Text] [Related]
16. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Orr HT; Chung MY; Banfi S; Kwiatkowski TJ; Servadio A; Beaudet AL; McCall AE; Duvick LA; Ranum LP; Zoghbi HY Nat Genet; 1993 Jul; 4(3):221-6. PubMed ID: 8358429 [TBL] [Abstract][Full Text] [Related]
17. Triplet repeat sequences in human DNA can be detected by hybridization to a synthetic (5'-CGG-3')17 oligodeoxyribonucleotide. Behn-Krappa A; Mollenhauer J; Doerfler W FEBS Lett; 1993 Nov; 333(3):248-50. PubMed ID: 8224187 [TBL] [Abstract][Full Text] [Related]
19. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome. Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; De Vos A; Platteau P; Lissens W; Van Steirteghem A; Liebaers I Mol Cell Endocrinol; 2001 Oct; 183 Suppl 1():S77-85. PubMed ID: 11576738 [TBL] [Abstract][Full Text] [Related]
20. [A new mechanism of mutation in man: expansion of trinucleotide repeats]. Illarioshkin SN; Ivanova-Smolenskaia IA; Markova ED Genetika; 1995 Nov; 31(11):1478-89. PubMed ID: 8666217 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]