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 *

109 related articles for article (PubMed ID: 8162064)

  • 1. Meiotic drive at the myotonic dystrophy locus?
    Carey N; Johnson K; Nokelainen P; Peltonen L; Savontaus ML; Juvonen V; Anvret M; Grandell U; Chotai K; Robertson E
    Nat Genet; 1994 Feb; 6(2):117-8. PubMed ID: 8162064
    [No Abstract]   [Full Text] [Related]  

  • 2. Meiotic drive and myotonic dystrophy.
    Hurst GD; Hurst LD; Barrett JA
    Nat Genet; 1995 Jun; 10(2):132-3. PubMed ID: 7663507
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophy.
    Barceló JM; Pluscauskas M; MacKenzie AE; Tsilfidis C; Narang M; Korneluk RG
    Am J Hum Genet; 1994 Jun; 54(6):1124-5. PubMed ID: 8198135
    [No Abstract]   [Full Text] [Related]  

  • 6. Brief report: reverse mutation in myotonic dystrophy.
    Brunner HG; Jansen G; Nillesen W; Nelen MR; de Die CE; Höweler CJ; van Oost BA; Wieringa B; Ropers HH; Smeets HJ
    N Engl J Med; 1993 Feb; 328(7):476-80. PubMed ID: 8421477
    [No Abstract]   [Full Text] [Related]  

  • 7. Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes.
    Thornton CA; Johnson K; Moxley RT
    Ann Neurol; 1994 Jan; 35(1):104-7. PubMed ID: 8285579
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Myotonic dystrophy--dynamic mutation and disease pathogenesis].
    Huminiecki L; Słomski R
    Postepy Biochem; 1997; 43(3):151-7. PubMed ID: 9558704
    [No Abstract]   [Full Text] [Related]  

  • 9. Human genetics. The costs of instability.
    Davies KE
    Nature; 1992 Mar; 356(6364):15. PubMed ID: 1538769
    [No Abstract]   [Full Text] [Related]  

  • 10. [Analysis of polymorphism of CTG repetitive sequences in the gene of myotonic dystrophy in human populations of the Volga-Ural region].
    Fatkhlislamova RI; Khidiatova IM; Khusnutdinova EK; Popova SN; Slominskiĭ PA; Limborskaia SA
    Genetika; 1999 Jul; 35(7):988-93. PubMed ID: 10519076
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trinucleotide repeat instability: when and where?
    Nelson DL; Warren ST
    Nat Genet; 1993 Jun; 4(2):107-8. PubMed ID: 8348143
    [No Abstract]   [Full Text] [Related]  

  • 12. [Genetic studies in the neuropsychiatric disorders].
    Kondo I
    Tanpakushitsu Kakusan Koso; 1993 Feb; 38(3):327-34. PubMed ID: 8488267
    [No Abstract]   [Full Text] [Related]  

  • 13. Centromere-associated female meiotic drive entails male fitness costs in monkeyflowers.
    Fishman L; Saunders A
    Science; 2008 Dec; 322(5907):1559-62. PubMed ID: 19056989
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Thornton-Griggs-Moxley disease: myotonic dystrophy type 2.
    Rowland LP
    Ann Neurol; 1994 Nov; 36(5):803-4. PubMed ID: 7979231
    [No Abstract]   [Full Text] [Related]  

  • 15. Retreat of the triplet repeat?
    Brook JD
    Nat Genet; 1993 Apr; 3(4):279-81. PubMed ID: 7981744
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. The diagnosis of myotonic dystrophy.
    Turnpenny PD; Kelly KF
    Scott Med J; 1993 Apr; 38(2):35-6. PubMed ID: 8502974
    [No Abstract]   [Full Text] [Related]  

  • 18. Mutable mutation. Some genes cause diseases by growing and growing and..
    Rennie J
    Sci Am; 1992 May; 266(5):34. PubMed ID: 1566039
    [No Abstract]   [Full Text] [Related]  

  • 19. Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene.
    Sabouri LA; Mahadevan MS; Narang M; Lee DS; Surh LC; Korneluk RG
    Nat Genet; 1993 Jul; 4(3):233-8. PubMed ID: 8358430
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tetrasomy 18p caused by paternal meiotic nondisjunction.
    Eggermann T; Engels H; Apacik C; Moskalonek B; Müller-Navia J; Schwanitz G; Stengel-Rutkowski S
    Eur J Hum Genet; 1997; 5(3):175-7. PubMed ID: 9272743
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.