BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 2361046)

  • 1. [Genetic analysis of Spanish families with myotonic dystrophy].
    Cobo AM; Martínez JM; Pradas J; Baiget M
    Neurologia; 1990 Mar; 5(3):86-91. PubMed ID: 2361046
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Prenatal diagnosis of myotonic dystrophy: the first experience in Spain].
    Cobo AM; Martínez JM; Parra J; Pérez MM; Pradas J; Baiget M
    Med Clin (Barc); 1990 Apr; 94(14):538-40. PubMed ID: 2355772
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies.
    Speer MC; Pericak-Vance MA; Yamaoka L; Hung WY; Ashley A; Stajich JM; Roses AD
    Neurology; 1990 Apr; 40(4):671-6. PubMed ID: 2320244
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The use of apolipoprotein CII as a genetic marker for myotonic dystrophy.
    Bird TD; Boehnke M; Schellenberg GD; Deeb SS; Lipe HP
    Arch Neurol; 1987 Mar; 44(3):273-5. PubMed ID: 2881531
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
    Reardon W; Floyd JL; Myring J; Lazarou LP; Meredith AL; Harper PS
    Am J Med Genet; 1992 Aug; 43(6):1006-11. PubMed ID: 1415325
    [TBL] [Abstract][Full Text] [Related]  

  • 7. "Shake hands"; diagnosing a floppy infant--myotonic dystrophy and the congenital subtype: a difficult perinatal diagnosis.
    Verrijn Stuart AA; Huisman M; van Straaten HL; Bakker JC; Arabin B
    J Perinat Med; 2000; 28(6):497-501. PubMed ID: 11155437
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Advances in myotonic dystrophy: a clinical and genetic perspective.
    Reardon W; Harper PS
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):605-9. PubMed ID: 1392133
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Myotonic dystrophy. Genetic, neonatologic and neuropsychological aspects].
    Olsen NK
    Ugeskr Laeger; 1989 Dec; 151(49):3300-3. PubMed ID: 2603228
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosis.
    Can B; Schaefer FV; Malik S; Floyd M; Say B
    J Okla State Med Assoc; 1998; 91(1):7-10. PubMed ID: 9503753
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers.
    Lavedan C; Hofmann H; Shelbourne P; Duros C; Savoy D; Johnson K; Junien C
    J Med Genet; 1991 Feb; 28(2):89-91. PubMed ID: 2002492
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers.
    Norman AM; Floyd JL; Meredith AL; Harper PS
    J Med Genet; 1989 Dec; 26(12):750-4. PubMed ID: 2575669
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic counselling for myotonic dystrophy: a comparison of lens examination and DNA linkage studies.
    Longstaff S; Curtis D; Quick J; Talbot J
    Eye (Lond); 1991; 5 ( Pt 1)():93-8. PubMed ID: 1676377
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.
    Myring J; Meredith AL; Harley HG; Kohn G; Norbury G; Harper PS; Shaw DJ
    J Med Genet; 1992 Nov; 29(11):785-8. PubMed ID: 1453427
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genotype-phenotype correlation in myotonic dystrophy and prediction of clinical seriousness].
    García-Gómez T; Maestre J; Garrido ML; Vilches R; Fernández MD; Mínguez A; Serrano P
    Rev Neurol; 1999 Sep 16-30; 29(6):499-502. PubMed ID: 10584260
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Direct diagnosis of myotonic dystrophy with a disease-specific DNA marker.
    Shelbourne P; Davies J; Buxton J; Anvret M; Blennow E; Bonduelle M; Schmedding E; Glass I; Lindenbaum R; Lane R
    N Engl J Med; 1993 Feb; 328(7):471-5. PubMed ID: 8421476
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Myotonic dystrophy in infancy and childhood.
    Hanson PA
    Pediatr Ann; 1984 Feb; 13(2):123-4, 126. PubMed ID: 6709403
    [No Abstract]   [Full Text] [Related]  

  • 19. Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.
    Mulley JC; Gedeon AK; White SJ; Haan EA; Richards RI
    J Med Genet; 1991 Jul; 28(7):448-52. PubMed ID: 1895314
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Myotonic dystrophy: opportunities for prenatal prediction.
    Schrott HG; Omenn GS
    Neurology; 1975 Aug; 25(8):789-91. PubMed ID: 1171415
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.