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26. Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases. Goldberg YP; Andrew SE; Theilmann J; Kremer B; Squitieri F; Telenius H; Brown JD; Hayden MR J Med Genet; 1993 Dec; 30(12):987-90. PubMed ID: 8133509 [TBL] [Abstract][Full Text] [Related]
27. [From gene to disease; HD gene and Huntington disease]. Maat-Kievit JA; Losekoot M; Roos RA Ned Tijdschr Geneeskd; 2001 Nov; 145(44):2120-3. PubMed ID: 11723754 [TBL] [Abstract][Full Text] [Related]
28. Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number. Rubinsztein DC; Barton DE; Davison BC; Ferguson-Smith MA Hum Mol Genet; 1993 Oct; 2(10):1713-5. PubMed ID: 8268927 [No Abstract] [Full Text] [Related]
29. Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families. Nørremølle A; Riess O; Epplen JT; Fenger K; Hasholt L; Sørensen SA Hum Mol Genet; 1993 Sep; 2(9):1475-6. PubMed ID: 8242074 [TBL] [Abstract][Full Text] [Related]
30. Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia. Rubinsztein DC; Leggo J; Goodburn S; Crow TJ; Lofthouse R; DeLisi LE; Barton DE; Ferguson-Smith MA J Med Genet; 1994 Sep; 31(9):690-3. PubMed ID: 7815437 [TBL] [Abstract][Full Text] [Related]
31. Mutation analysis in patients with possible but apparently sporadic Huntington's disease. Davis MB; Bateman D; Quinn NP; Marsden CD; Harding AE Lancet; 1994 Sep; 344(8924):714-7. PubMed ID: 7915776 [TBL] [Abstract][Full Text] [Related]
32. Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene. Zühlke C; Riess O; Bockel B; Lange H; Thies U Hum Mol Genet; 1993 Dec; 2(12):2063-7. PubMed ID: 8111374 [TBL] [Abstract][Full Text] [Related]
33. Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects. Goldberg YP; Kremer B; Andrew SE; Theilmann J; Graham RK; Squitieri F; Telenius H; Adam S; Sajoo A; Starr E Nat Genet; 1993 Oct; 5(2):174-9. PubMed ID: 8252043 [TBL] [Abstract][Full Text] [Related]
34. Huntington's Disease: Relationship Between Phenotype and Genotype. Sun YM; Zhang YB; Wu ZY Mol Neurobiol; 2017 Jan; 54(1):342-348. PubMed ID: 26742514 [TBL] [Abstract][Full Text] [Related]
35. Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease. Riess O; Noerremoelle A; Soerensen SA; Epplen JT Hum Mol Genet; 1993 Sep; 2(9):1523. PubMed ID: 8242095 [No Abstract] [Full Text] [Related]
36. Transglutaminase activity is related to CAG repeat length in patients with Huntington's disease. Cariello L; de Cristofaro T; Zanetti L; Cuomo T; Di Maio L; Campanella G; Rinaldi S; Zanetti P; Di Lauro R; Varrone S Hum Genet; 1996 Dec; 98(6):633-5. PubMed ID: 8931689 [TBL] [Abstract][Full Text] [Related]
37. Does mRNA translation starting from an alternative initiation site contribute to the pathology of Huntington's disease? Santos AD; Padlan EA Med Hypotheses; 2000 May; 54(5):689-90. PubMed ID: 10859666 [TBL] [Abstract][Full Text] [Related]
38. Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. Hummerich H; Baxendale S; Mott R; Kirby SF; MacDonald ME; Gusella J; Lehrach H; Bates GP Hum Mol Genet; 1994 Jan; 3(1):73-8. PubMed ID: 8162055 [TBL] [Abstract][Full Text] [Related]
39. The enigma of Huntington's disease. Cattaneo E; Rigamonti D; Zuccato C Sci Am; 2002 Dec; 287(6):92-7. PubMed ID: 12469651 [No Abstract] [Full Text] [Related]
40. [Huntington's disease: molecular basis and detection of carriers]. Bogolobov A; Frydmann M; Lubomirov L; Borochovitz Z; Fried K; Dangur N; Gazit E Harefuah; 1996 Feb; 130(3):152-7; 224. PubMed ID: 8682389 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]