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 *

120 related articles for article (PubMed ID: 1338761)

  • 1. Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat.
    Crow SR; Harley HG; Brook JD; Rundle SA; Shaw DJ
    Hum Mol Genet; 1992 Sep; 1(6):451. PubMed ID: 1338761
    [No Abstract]   [Full Text] [Related]  

  • 2. Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.
    Rubinsztein DC; Leggo J; Amos W; Barton DE; Ferguson-Smith MA
    Hum Mol Genet; 1994 Nov; 3(11):2031-5. PubMed ID: 7874122
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Origin of the expansion mutation in myotonic dystrophy.
    Imbert G; Kretz C; Johnson K; Mandel JL
    Nat Genet; 1993 May; 4(1):72-6. PubMed ID: 8513329
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) gene.
    Jansen G; Coerwinkel-Driessen M; Nillesen W; Brunner H; Wieringa B
    Hum Mol Genet; 1993 Mar; 2(3):333. PubMed ID: 8499928
    [No Abstract]   [Full Text] [Related]  

  • 5. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.
    Mahadevan M; Tsilfidis C; Sabourin L; Shutler G; Amemiya C; Jansen G; Neville C; Narang M; Barceló J; O'Hoy K
    Science; 1992 Mar; 255(5049):1253-5. PubMed ID: 1546325
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy.
    Mahadevan MS; Foitzik MA; Surh LC; Korneluk RG
    Genomics; 1993 Feb; 15(2):446-8. PubMed ID: 8449517
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period.
    Martorell L; Martinez JM; Carey N; Johnson K; Baiget M
    J Med Genet; 1995 Aug; 32(8):593-6. PubMed ID: 7473648
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.
    Tsilfidis C; MacKenzie AE; Mettler G; Barceló J; Korneluk RG
    Nat Genet; 1992 Jun; 1(3):192-5. PubMed ID: 1303233
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Myotonic dystrophy reviewed: back to the future?
    Wieringa B
    Hum Mol Genet; 1994 Jan; 3(1):1-7. PubMed ID: 8162011
    [No Abstract]   [Full Text] [Related]  

  • 10. An unstable triplet repeat in a gene related to myotonic muscular dystrophy.
    Fu YH; Pizzuti A; Fenwick RG; King J; Rajnarayan S; Dunne PW; Dubel J; Nasser GA; Ashizawa T; de Jong P
    Science; 1992 Mar; 255(5049):1256-8. PubMed ID: 1546326
    [TBL] [Abstract][Full Text] [Related]  

  • 11. French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion.
    Lavedan C; Hofmann-Radvanyi H; Boileau C; Bonaïti-Pellié C; Savoy D; Shelbourne P; Duros C; Rabes JP; Dehaupas I; Luce S
    J Med Genet; 1994 Jan; 31(1):33-6. PubMed ID: 8151634
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.
    Hunter AG; Jacob P; O'Hoy K; MacDonald I; Mettler G; Tsilfidis C; Korneluk RG
    Am J Med Genet; 1993 Feb; 45(3):401-7. PubMed ID: 8434633
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Advances in molecular genetics of myotonic dystrophy].
    Yamagata H; Yamanaka N; Miki T; Ogihara T
    Nihon Rinsho; 1993 Sep; 51(9):2474-80. PubMed ID: 8411731
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unstable DNA sequence in myotonic dystrophy.
    Harley HG; Rundle SA; Reardon W; Myring J; Crow S; Brook JD; Harper PS; Shaw DJ
    Lancet; 1992 May; 339(8802):1125-8. PubMed ID: 1349364
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myotonic dystrophy: correlation of clinical symptoms with the size of the CTG trinucleotide repeat.
    Jaspert A; Fahsold R; Grehl H; Claus D
    J Neurol; 1995 Jan; 242(2):99-104. PubMed ID: 7707098
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.
    Shaw DJ; Meredith AL; Sarfarazi M; Harley HG; Huson SM; Brook JD; Bufton L; Litt M; Mohandas T; Harper PS
    Hum Genet; 1986 Nov; 74(3):262-6. PubMed ID: 2877933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy.
    Wenger SL; Giangreco CA; Tarleton J; Wessel HB
    Am J Med Genet; 1996 Dec; 66(1):60-3. PubMed ID: 8957513
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CTG trinucleotide repeat variability in identical twins with myotonic dystrophy.
    López de Munain A; Cobo AM; Huguet E; Marti Massó JF; Johnson K; Baiget M
    Ann Neurol; 1994 Mar; 35(3):374-5. PubMed ID: 8122893
    [No Abstract]   [Full Text] [Related]  

  • 19. Six transcripts map within 200 kilobases of the myotonic dystrophy expanded repeat.
    Alwazzan M; Hamshere MG; Lennon GG; Brook JD
    Mamm Genome; 1998 Jun; 9(6):485-7. PubMed ID: 9585442
    [No Abstract]   [Full Text] [Related]  

  • 20. Myotonic dystrophy and limb girdle muscular dystrophy in one family.
    Schröder R; Beyenburg S; Weber J; Olek K; Zierz S
    Clin Investig; 1994 May; 72(5):409-13. PubMed ID: 8086779
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.