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 *

128 related articles for article (PubMed ID: 6134107)

  • 1. Carrier detection in Duchenne muscular dystrophy by use of cloned DNA sequences.
    Wieacker P; Davies K; Pearson P; Ropers HH
    Lancet; 1983 Jun; 1(8337):1325-6. PubMed ID: 6134107
    [No Abstract]   [Full Text] [Related]  

  • 2. Molecular analysis of the Duchenne muscular dystrophy locus.
    Honeycombe J; Anand R
    Comp Biochem Physiol A Comp Physiol; 1989; 93(1):125-31. PubMed ID: 2568215
    [No Abstract]   [Full Text] [Related]  

  • 3. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy.
    Murray JM; Davies KE; Harper PS; Meredith L; Mueller CR; Williamson R
    Nature; 1982 Nov; 300(5887):69-71. PubMed ID: 6982420
    [No Abstract]   [Full Text] [Related]  

  • 4. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF; Harris SG; Tsao CC; Ward PA; Caskey CT
    Neurology; 1986 Dec; 36(12):1553-62. PubMed ID: 2878392
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Carrier detection and gene analysis of Duchenne muscular dystrophy.
    Pearson PL; van Ommen GJ; Bakker E
    Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():353-8. PubMed ID: 2884063
    [No Abstract]   [Full Text] [Related]  

  • 6. Duchenne muscular dystrophy: carrier detection by ultrasound.
    Steinbicker V; von Rohden L; Krebs P; Szibor R
    Lancet; 1984 Jun; 1(8392):1463. PubMed ID: 6145895
    [No Abstract]   [Full Text] [Related]  

  • 7. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.
    Old JM; Davies KE
    J Med Genet; 1986 Dec; 23(6):556-9. PubMed ID: 2879927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cloned gene probes for carrier detection in muscular dystrophy.
    Davies KE; Harper PS; Williamson R
    Lancet; 1983 Jul; 2(8341):108. PubMed ID: 6134944
    [No Abstract]   [Full Text] [Related]  

  • 9. Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.
    Yau SC; Roberts RG; Bobrow M; Mathew CG
    Lancet; 1993 Jan; 341(8840):273-5. PubMed ID: 8093919
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.
    Emery AE
    Br Med Bull; 1980 May; 36(2):117-22. PubMed ID: 7020836
    [No Abstract]   [Full Text] [Related]  

  • 11. Detection of carriers of human Duchenne muscular dystrophy by freeze-fracture analysis of erythrocyte plasmalemmal intramembrane particles.
    Shivers RR; Martin K; Atkinson BG
    Am J Clin Pathol; 1986 Feb; 85(2):131-4. PubMed ID: 3946298
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis and diagnosis of Duchenne muscular dystrophy.
    Forrest SM; Smith TJ; Cross GS; Kenwrick SJ; England S; Flint T; Davies KE
    J R Coll Physicians Lond; 1988 Apr; 22(2):65-7. PubMed ID: 3294388
    [No Abstract]   [Full Text] [Related]  

  • 13. Carrier detection in Duchenne muscular dystropy.
    Tagliavini J; Ottonello S; Grassi E; Marchini C; Rossi GL; Lucci B; Parma M; Reggiani R
    Neurology; 1979 Oct; 29(10):1423-5. PubMed ID: 573388
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duchenne muscular dystrophy. Use of rubidium chloride Rb 86 in the detection of carriers of the gene.
    Bradley WG; Gardner-Medwin D; Haggith J; Walton JN; Hesp R
    Arch Neurol; 1971 Sep; 25(3):193-7. PubMed ID: 4951942
    [No Abstract]   [Full Text] [Related]  

  • 15. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy.
    Hodgson SV; Bobrow M
    Br Med Bull; 1989 Jul; 45(3):719-44. PubMed ID: 2688825
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DNA analysis and genetic counselling in Duchenne muscular dystrophy.
    Gardner RJ; Wilson SJ; Wilkins RJ
    N Z Med J; 1988 Jul; 101(849):455-7. PubMed ID: 3399183
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.
    Speer A; Davies K; McGlade S; Hanke R; Spiegler AW; Szibor R; Sommer D; Herrmann F; Coutelle C
    Biomed Biochim Acta; 1986; 45(7):K19-27. PubMed ID: 2878658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular deletion analysis in Duchenne muscular dystrophy.
    Thomas NS; Ray PN; Worton RG; Harper PS
    J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNA probes for carrier identification in Duchenne muscular dystrophy.
    Worton RG
    Clin Chem; 1989 Apr; 35(4):519-20. PubMed ID: 2564816
    [No Abstract]   [Full Text] [Related]  

  • 20. Carrier detection in Duchenne muscular dystrophy: a review of current issues and approaches.
    Gruemer HD; Prior T
    Clin Chim Acta; 1987 Jan; 162(1):1-18. PubMed ID: 2879654
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.