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8. [The role of trinucleotide repeats in human genetic diseases]. Hietanen K Duodecim; 1996; 112(3):188-93. PubMed ID: 10590627 [No Abstract] [Full Text] [Related]
14. Analysis of triplet-repeat DNA by capillary electrophoresis. Kiba Y; Baba Y Methods Mol Biol; 2001; 163():221-9. PubMed ID: 11242947 [No Abstract] [Full Text] [Related]
17. Trinucleotide repeats: mechanisms and pathophysiology. Cummings CJ; Zoghbi HY Annu Rev Genomics Hum Genet; 2000; 1():281-328. PubMed ID: 11701632 [TBL] [Abstract][Full Text] [Related]
18. Triplet repeat mutations in human disease. Caskey CT; Pizzuti A; Fu YH; Fenwick RG; Nelson DL Science; 1992 May; 256(5058):784-9. PubMed ID: 1589758 [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. Trinucleotide repeat expansion and neuropsychiatric disease. Margolis RL; McInnis MG; Rosenblatt A; Ross CA Arch Gen Psychiatry; 1999 Nov; 56(11):1019-31. PubMed ID: 10565502 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]