These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 7760321)

  • 1. DNA analysis of Huntington's disease in southern Chinese.
    Chan V; Yu YL; Chan TP; Yip B; Chang CM; Wong MT; Chan YW; Chan TK
    J Med Genet; 1995 Feb; 32(2):120-4. PubMed ID: 7760321
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype.
    Rubinsztein DC; Leggo J; Goodburn S; Barton DE; Ferguson-Smith MA
    Hum Mol Genet; 1995 Feb; 4(2):203-6. PubMed ID: 7757068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
    De Rooij KE; De Koning Gans PA; Skraastad MI; Belfroid RD; Vegter-Van Der Vlis M; Roos RA; Bakker E; Van Ommen GJ; Den Dunnen JT; Losekoot M
    J Med Genet; 1993 Dec; 30(12):996-1002. PubMed ID: 8133511
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clustering of multiallele DNA markers near the Huntington's disease gene.
    MacDonald ME; Cheng SV; Zimmer M; Haines JL; Poustka A; Allitto B; Smith B; Whaley WL; Romano DM; Jagadeesh J
    J Clin Invest; 1989 Sep; 84(3):1013-6. PubMed ID: 2569477
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A study on Huntington's disease associated trinucleotide repeat within the Chinese population.
    Soong BW; Wang JT
    Proc Natl Sci Counc Repub China B; 1995 Jul; 19(3):137-42. PubMed ID: 7480359
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence.
    Squitieri F; Andrew SE; Goldberg YP; Kremer B; Spence N; Zeisler J; Nichol K; Theilmann J; Greenberg J; Goto J
    Hum Mol Genet; 1994 Dec; 3(12):2103-14. PubMed ID: 7881406
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
    Agostinho Lde A; Rocha CF; Medina-Acosta E; Barboza HN; da Silva AF; Pereira SP; da Silva Idos S; Paradela ER; Figueiredo AL; Nogueira Ede M; Alvarenga RM; Hernan Cabello P; dos Santos SR; Paiva CL
    J Hum Genet; 2012 Dec; 57(12):796-803. PubMed ID: 23051704
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease.
    Almqvist E; Spence N; Nichol K; Andrew SE; Vesa J; Peltonen L; Anvret M; Goto J; Kanazawa I; Goldberg YP
    Hum Mol Genet; 1995 Feb; 4(2):207-14. PubMed ID: 7757069
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene.
    Theilmann J; Kanani S; Shiang R; Robbins C; Quarrell O; Huggins M; Hedrick A; Weber B; Collins C; Wasmuth JJ
    J Med Genet; 1989 Nov; 26(11):676-81. PubMed ID: 2531224
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.
    Dodé C; Dürr A; Pêcheux C; Mouret JF; Belal S; Bachner L; Agid Y; Kaplan JC; Brice A; Feingold J
    C R Acad Sci III; 1993 Nov; 316(11):1374-80. PubMed ID: 8087617
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.
    Robbins C; Theilmann J; Youngman S; Haines J; Altherr MJ; Harper PS; Payne C; Junker A; Wasmuth J; Hayden MR
    Am J Hum Genet; 1989 Mar; 44(3):422-5. PubMed ID: 2521771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expansion of a (CAG)n repeat region in a sporadic case of HD.
    Bozza A; Malagù S; Calzolari E; Novelletto A; Pavoni M; del Senno L
    Acta Neurol Scand; 1995 Aug; 92(2):132-4. PubMed ID: 7484060
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.
    Masuda N; Goto J; Murayama N; Watanabe M; Kondo I; Kanazawa I
    J Med Genet; 1995 Sep; 32(9):701-5. PubMed ID: 8544189
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Molecular diagnosis of Huntington's disease: an analysis of two large families].
    Zeng Y; Chen M; Mao Y
    Zhonghua Yi Xue Za Zhi; 1995 Nov; 75(11):689-93, 711-2. PubMed ID: 8697093
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of CAG repeat expansion in Huntington's disease gene (IT 15) in a Hungarian population.
    Jakab K; Gárdián G; Endreffy E; Kalmár T; Bachrati C; Vécsei L; Raskó I
    Eur Neurol; 1999; 41(2):107-10. PubMed ID: 10023115
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Molecular genetics of Huntington's disease].
    Goto J; Masuda N; Watanabe M; Kanazawa I
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1529-31. PubMed ID: 8752453
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.