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 *

129 related articles for article (PubMed ID: 2905983)

  • 1. [DNA diagnosis of muscular dystrophies].
    Lindlöf M; Somer H
    Duodecim; 1988; 104(22):1787-95. PubMed ID: 2905983
    [No Abstract]   [Full Text] [Related]  

  • 2. Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism.
    Akita Y; Ohno S; Goto J; Nakano I; Takatsu M; Sugita H; Suzuki K
    Jinrui Idengaku Zasshi; 1987 Jun; 32(2):71-82. PubMed ID: 2893850
    [No Abstract]   [Full Text] [Related]  

  • 3. DMD carrier detection and prenatal diagnosis via recombinant DNA methods.
    Caskey CT; Ward P; Hejtmancik F
    Adv Neurol; 1988; 48():83-91. PubMed ID: 2891260
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. [The molecular principles of Duchenne and Becker muscular dystrophy and their genetic diagnosis].
    Speer A; Davies KE; Hanke R; Grade K; Spiegler AW; Herrmann FH; Szibor R; Wulff K; Sommer D; Metzke H
    Z Arztl Fortbild (Jena); 1989; 83(3):117-20. PubMed ID: 2655303
    [No Abstract]   [Full Text] [Related]  

  • 6. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC; Gedeon AK; Haan EA; Sheffield LJ; White SJ; Bates LJ; Robertson EF; Sutherland GR
    Aust Paediatr J; 1988; 24 Suppl 1():92-7. PubMed ID: 3202740
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms.
    Romeo G; Rocchi M; Roncuzzi L; Ferlini A; Nobile C; Rugolo M
    Adv Neurol; 1988; 48():31-6. PubMed ID: 2891257
    [No Abstract]   [Full Text] [Related]  

  • 8. Gene mapping and the muscular dystrophies.
    Harper PS
    Prog Clin Biol Res; 1989; 306():29-49. PubMed ID: 2567999
    [No Abstract]   [Full Text] [Related]  

  • 9. X;autosome translocations in females with Duchenne or Becker muscular dystrophy.
    Dubowitz V
    Nature; 1986 Jul 17-23; 322(6076):291-2. PubMed ID: 3461282
    [No Abstract]   [Full Text] [Related]  

  • 10. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S; Shukin RJ; McGillivray BC; Ray PN; Worton RG
    Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M
    Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy].
    Graninger W; Wintersberger W; Meron G; Smolen J; Toifl K; Vormittag W
    Wien Klin Wochenschr; 1991; 103(7):207-9. PubMed ID: 2063586
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Etiology of numerical and structural aberrations of the X chromosome. A study with highly polymorphic DNA markers].
    Lorda-Sanchez I; Schinzel AA
    Ergeb Inn Med Kinderheilkd; 1993; 61():57-121. PubMed ID: 7900996
    [No Abstract]   [Full Text] [Related]  

  • 14. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
    Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH
    Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797
    [No Abstract]   [Full Text] [Related]  

  • 15. [Differential diagnosis of a benign course of muscular dystrophy using molecular genetic methods].
    Wagner M; Diedrich U; Pozsàr C; Becker PE; Reiss J
    Nervenarzt; 1990 Apr; 61(4):244-7. PubMed ID: 2352571
    [No Abstract]   [Full Text] [Related]  

  • 16. [Presentation of a complex monitoring and therapy program in neuromuscular diseases, exemplified by X chromosomal muscular dystrophies. 1: Etiology, development, clinical and paraclinical findings].
    Hoffmann W; Ullrich KP
    Padiatr Grenzgeb; 1987; 26(4):271-8. PubMed ID: 3658476
    [No Abstract]   [Full Text] [Related]  

  • 17. Linkage analyses in families with nephrogenic diabetes insipidus.
    Knoers NV; van der Heyden H; van Oost BA; Monnens L; Willems J; Ropers HH
    Prog Clin Biol Res; 1989; 305():149-55. PubMed ID: 2569742
    [No Abstract]   [Full Text] [Related]  

  • 18. [Principles of DNA diagnosis].
    Moser H
    Klin Monbl Augenheilkd; 1990 May; 196(5):265-8. PubMed ID: 2366450
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Use of DNA analysis in the prevention of progressive muscular dystrophies].
    Kádasi L; Ferák V; Thurzová M; Kvasnicová M
    Bratisl Lek Listy; 1988 Nov; 89(11):828-34. PubMed ID: 2904832
    [No Abstract]   [Full Text] [Related]  

  • 20. [DNA markers, genetic counseling and prenatal diagnosis of hereditary disease. A study of 3 families with Duchenne's muscular dystrophy].
    Schwartz M; Nørby S; Brandt NJ
    Ugeskr Laeger; 1985 Jun; 147(26):2071-5. PubMed ID: 3863357
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.