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 *

98 related articles for article (PubMed ID: 466851)

  • 41. Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy.
    Ricker K; Koch MC; Lehmann-Horn F; Pongratz D; Speich N; Reiners K; Schneider C; Moxley RT
    Arch Neurol; 1995 Jan; 52(1):25-31. PubMed ID: 7826272
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype.
    Larsen M; Kress W; Schoser B; Hehr U; Müller CR; Rost S
    Eur J Hum Genet; 2016 Oct; 24(10):1467-72. PubMed ID: 27222292
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion].
    Zhao XP; Xie HJ; Zheng HM; Yu ZL; Cui Y; Ding SJ; Ren DM; Tang GM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):459-62. PubMed ID: 15476170
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM).
    Greiner J; Spengler DH; Krüger J; Tariverdian G
    Hum Genet; 1988 Apr; 78(4):330-2. PubMed ID: 3162894
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Clinical, familial and hereditary analysis of myotonic dystrophy].
    Wu Z; Yang J; Cao J; Hu Z; Zhan Y; Li J; Li Y; Wang Y; Zhang C
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun; 36(6):520-4. PubMed ID: 21743143
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Blood group antigens and ABH secretor status in dystrophia myotonica (Curschmann-Steinert)].
    Mielke U; Gramer L; Schimrigk K
    Klin Padiatr; 1986; 198(4):312-5. PubMed ID: 3762003
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The DM mutation; diagnostic applications in the Finnish population.
    Nokelainen P; Shelbourne P; Shaw D; Brook JD; Harley HG; Johnson K; Somer H; Savontaus ML; Peltonen L
    Clin Genet; 1993 Apr; 43(4):190-5. PubMed ID: 8101149
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Application of the polymerase chain reaction technique (PCR) to the molecular diagnosis of myotonic dystrophy].
    Cobo AM; Martínez JM; López de Munain A; Baiget M
    Neurologia; 1991 Nov; 6(9):317-21. PubMed ID: 1687310
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.
    Gennarelli M; Novelli G; Cobo A; Baiget M; Dallapiccola B
    Hum Genet; 1991 Oct; 87(6):654-6. PubMed ID: 1682233
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Linkage of the LW blood group locus with the complement C3 and Lutheran blood group loci.
    Sistonen P
    Ann Hum Genet; 1984 Jul; 48(3):239-42. PubMed ID: 6431896
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Genetic and physical demarcation of the locus for dystrophia myotonica.
    Wieringa B; Brunner H; Hulsebos T; Schonk D; Ropers HH
    Adv Neurol; 1988; 48():47-69. PubMed ID: 2891258
    [No Abstract]   [Full Text] [Related]  

  • 52. The Lutheran and secretor loci: genetic linkage analysis.
    Lewis M; Kaita H; Chown B; Giblett ER; Anderson J; Côté GB
    Am J Hum Genet; 1977 Jan; 29(1):101-6. PubMed ID: 835569
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Characteristics of myotonic dystrophy in Istria: molecular genetic approach. Part II: Analysis of genetic polymorphisms.
    Medica I; Logar N; Peterlin B
    Coll Antropol; 2000 Dec; 24(2):287-94. PubMed ID: 11216395
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Presymptomatic diagnosis of myotonic dystrophy.
    Brunner HG; Nillesen W; van Oost BA; Jansen G; Wieringa B; Ropers HH; Smeets HJ
    J Med Genet; 1992 Nov; 29(11):780-4. PubMed ID: 1453426
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Presymptomatic exclusion of myotonic dystrophy in a one-generation pedigree of half-siblings.
    Ott J; Caesar J; Mächler M; Schinzel A; Schmid W
    Hum Hered; 1990; 40(5):305-7. PubMed ID: 2265856
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Cataract and myotonic dystrophy: the role of molecular diagnosis.
    Reardon W; MacMillan JC; Myring J; Harley HG; Rundle SA; Beck L; Harper PS; Shaw DJ
    Br J Ophthalmol; 1993 Sep; 77(9):579-83. PubMed ID: 8218057
    [TBL] [Abstract][Full Text] [Related]  

  • 57. High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation.
    Neville CE; Mahadevan MS; Barceló JM; Korneluk RG
    Hum Mol Genet; 1994 Jan; 3(1):45-51. PubMed ID: 7909252
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMM.
    Sun C; Henriksen OA; Tranebjaerg L
    Clin Genet; 1999 Dec; 56(6):457-61. PubMed ID: 10665666
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers.
    Takemoto Y; Miki T; Nakura J; Nishikawa K; Kamino K; Takeda S; Kuzu K; Osame M; Nakagawa M; Higuchi I
    Jinrui Idengaku Zasshi; 1989 Sep; 34(3):189-94. PubMed ID: 2576756
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci.
    Harper PS; Rivas ML; Bias WB; Hutchinson JR; Dyken PR; McKusick VA
    Am J Hum Genet; 1972 May; 24(3):310-6. PubMed ID: 5063795
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.