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 *

123 related articles for article (PubMed ID: 7760317)

  • 21. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.
    Harley HG; Rundle SA; MacMillan JC; Myring J; Brook JD; Crow S; Reardon W; Fenton I; Shaw DJ; Harper PS
    Am J Hum Genet; 1993 Jun; 52(6):1164-74. PubMed ID: 8503448
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An intergenerational contraction of the CTG repeat in Japanese myotonic dystrophy.
    Matsumura R; Namikawa T; Miki T; Kihira T; Yamagata H; Mano Y; Takayanagi T
    J Neurol Sci; 1996 Jul; 139(1):48-51. PubMed ID: 8836971
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Dynamic balance of segregation distortion and selection maintains normal allele sizes at the myotonic dystrophy locus.
    Polański A; Chakraborty R; Kimmel M; Deka R
    Math Biosci; 1998 Jan; 147(1):93-112. PubMed ID: 9401353
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Origin of a regressed myotonic dystrophy allele.
    Giordano M; De Angelis MS; Mutani R; Richiardi PM
    J Med Genet; 1994 Feb; 31(2):130-2. PubMed ID: 8182718
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions.
    Pešović J; Perić S; Brkušanin M; Brajušković G; Rakočević-Stojanović V; Savić-Pavićević D
    Neurogenetics; 2017 Dec; 18(4):207-218. PubMed ID: 28942489
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Orthopaedic manifestations of congenital myotonic dystrophy during childhood and adolescence.
    Canavese F; Sussman MD
    J Pediatr Orthop; 2009 Mar; 29(2):208-13. PubMed ID: 19352249
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis in myotonic dystrophy type 1. Thirteen years of experience: implications for reproductive counselling in DM1 families.
    Martorell L; Cobo AM; Baiget M; Naudó M; Poza JJ; Parra J
    Prenat Diagn; 2007 Jan; 27(1):68-72. PubMed ID: 17154336
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Direct genotype analysis in congenital myotonic dystrophy with an unusual family anamnesis].
    Bindl L; Rummel W; Walter S; Haverkamp F; Kowalewski S; Lentze MJ; Koch M
    Klin Padiatr; 1993; 205(5):367-9. PubMed ID: 8411905
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CTG repeat number at the myotonic dystrophy locus in healthy Kuwaiti individuals: possible explanation of why myotonic dystrophy is rare in Kuwait.
    Alfadhli S; Elshafey AE; Bastaki L; Al-Awadi S
    Arch Neurol; 2004 Jun; 61(6):895-8. PubMed ID: 15210527
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
    Braida C; Stefanatos RK; Adam B; Mahajan N; Smeets HJ; Niel F; Goizet C; Arveiler B; Koenig M; Lagier-Tourenne C; Mandel JL; Faber CG; de Die-Smulders CE; Spaans F; Monckton DG
    Hum Mol Genet; 2010 Apr; 19(8):1399-412. PubMed ID: 20080938
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Contrasts in clinical presentation and genetic transmission of myotonic dystrophy.
    Reifer H; Sobel E
    J Am Podiatr Med Assoc; 1998 Jul; 88(7):313-22. PubMed ID: 9680767
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat.
    Ashizawa T; Dubel JR; Dunne PW; Dunne CJ; Fu YH; Pizzuti A; Caskey CT; Boerwinkle E; Perryman MB; Epstein HF
    Neurology; 1992 Oct; 42(10):1877-83. PubMed ID: 1407566
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutagenic stress modulates the dynamics of CTG repeat instability associated with myotonic dystrophy type 1.
    Piñeiro E; Fernàndez-López L; Gamez J; Marcos R; Surrallés J; Velázquez A
    Nucleic Acids Res; 2003 Dec; 31(23):6733-40. PubMed ID: 14627806
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital myotonic dystrophy in Britain. II. Genetic basis.
    Harper PS
    Arch Dis Child; 1975 Jul; 50(7):514-21. PubMed ID: 1167063
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated cases.
    Martorell L; Illa I; Rosell J; Benitez J; Sedano MJ; Baiget M
    J Med Genet; 1996 Sep; 33(9):783-5. PubMed ID: 8880582
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Congenital myotonic dystrophy. Incidence, clinical aspects and early prognosis.
    Wesström G; Bensch J; Schollin J
    Acta Paediatr Scand; 1986 Sep; 75(5):849-54. PubMed ID: 3564952
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Congenital myotonic dystrophy: molecular diagnosis and clinical study.
    Hojo K; Yamagata H; Moji H; Fujita T; Miki T; Fujimura M; Kidoguchi K
    Am J Perinatol; 1995 May; 12(3):195-200. PubMed ID: 7612095
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Transmission ratio distortion in the myotonic dystrophy locus in human preimplantation embryos.
    Dean NL; Loredo-Osti JC; Fujiwara TM; Morgan K; Tan SL; Naumova AK; Ao A
    Eur J Hum Genet; 2006 Mar; 14(3):299-306. PubMed ID: 16391559
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Somatic cell heterogeneity between DNA extracted from lymphocytes and skeletal muscle in congenital myotonic dystrophy.
    Ohya K; Tachi N; Kon S; Kikuchi K; Chiba S
    Jpn J Hum Genet; 1995 Dec; 40(4):319-26. PubMed ID: 8851765
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.