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14. [Triplet repeat expansions in hereditary neurodegenerative diseases]. Peñuelas I; de Miguel C; Gullón A Med Clin (Barc); 1997 Apr; 108(14):542-8. PubMed ID: 9190441 [No 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. 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]
17. Mental status and fragile X expression in relation to FMR-1 gene mutation. de Vries BB; Wiegers AM; de Graaff E; Verkerk AJ; Van Hemel JO; Halley DJ; Fryns JP; Curfs LM; Niermeijer MF; Oostra BA Eur J Hum Genet; 1993; 1(1):72-9. PubMed ID: 8069653 [TBL] [Abstract][Full Text] [Related]
18. Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome. Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJ; Horst J; Mazurczak T Acta Biochim Pol; 1996; 43(2):383-8. PubMed ID: 8862184 [TBL] [Abstract][Full Text] [Related]
19. FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male. Loesch DZ J Med Genet; 1997 Apr; 34(4):350. PubMed ID: 9138164 [No Abstract] [Full Text] [Related]
20. Simple tandem DNA repeats and human genetic disease. Sutherland GR; Richards RI Proc Natl Acad Sci U S A; 1995 Apr; 92(9):3636-41. PubMed ID: 7731957 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]