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Journal Abstract Search

168 related items for PubMed ID: 2891253

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. [Problems and peculiarities in establishing the genealogical findings and the genetic counseling in hereditary neuromuscular diseases].
    Bachmann H, Lössner J.
    Z Gesamte Inn Med; 1981 Jun 01; 36(11):381-6. PubMed ID: 7303764
    [Abstract] [Full Text] [Related]

  • 4. [Diagnosis of Duchenne muscular dystrophy using DNA probes].
    Evgrafov OV, Makarov VB.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1987 Jun 01; 87(11):1732-6. PubMed ID: 3324590
    [No Abstract] [Full Text] [Related]

  • 5. [Diagnosis of neuromuscular diseases: progress with molecular genetic techniques].
    Gencik M, Epplen JT, Mortier W.
    Dtsch Med Wochenschr; 1999 Jan 29; 124(4):85-7. PubMed ID: 10071605
    [No Abstract] [Full Text] [Related]

  • 6. Genetic considerations in neuromuscular diseases.
    Rowley PT.
    Adv Neurol; 1977 Jan 29; 17():227-33. PubMed ID: 888737
    [No Abstract] [Full Text] [Related]

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    ; . PubMed ID:
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  • 9. [Neuromuscular diseases. Molecular genetic methods will revolutionize diagnosis and treatment].
    Anvret M, Edström L, Ahlberg G.
    Lakartidningen; 1992 Mar 11; 89(11):862, 865-9. PubMed ID: 1545641
    [No Abstract] [Full Text] [Related]

  • 10. 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 Mar 11; 5(2):183-5. PubMed ID: 7917130
    [Abstract] [Full Text] [Related]

  • 11. 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 Mar 11; 48():31-6. PubMed ID: 2891257
    [No Abstract] [Full Text] [Related]

  • 12. DNA analysis and genetic counselling in Duchenne muscular dystrophy.
    Gardner RJ, Wilson SJ, Wilkins RJ.
    N Z Med J; 1988 Jul 13; 101(849):455-7. PubMed ID: 3399183
    [Abstract] [Full Text] [Related]

  • 13. [DNA diagnosis of muscular dystrophies].
    Lindlöf M, Somer H.
    Duodecim; 1988 Jul 13; 104(22):1787-95. PubMed ID: 2905983
    [No Abstract] [Full Text] [Related]

  • 14. Modern genetics and neuromuscular disorders.
    Lancet; 1987 Mar 14; 1(8533):626-7. PubMed ID: 2881158
    [No Abstract] [Full Text] [Related]

  • 15. [Diagnostic studies in patients and relatives with hereditary neuromuscular diseases].
    Moser H.
    Ther Umsch; 1995 Dec 14; 52(12):810-3. PubMed ID: 8539652
    [Abstract] [Full Text] [Related]

  • 16. [DNA markers, genetic counseling and prenatal diagnosis of hereditary diseases. A study of 3 families with Duchenne's muscular dystrophy].
    Schwartz M, Nørby S, Brandt NJ.
    Ugeskr Laeger; 1985 Jul 22; 147(30):2382-6. PubMed ID: 3864307
    [No Abstract] [Full Text] [Related]

  • 17. [In which cases does molecular biology allow a diagnosis in neuromuscular pathology?].
    Pouget J.
    Rev Neurol (Paris); 2009 Apr 22; 165 Spec No 2():F73-9. PubMed ID: 19593880
    [No Abstract] [Full Text] [Related]

  • 18. [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 24; 147(26):2071-5. PubMed ID: 3863357
    [No Abstract] [Full Text] [Related]

  • 19. [Problem of phenotypic polymorphism in hereditary neuromuscular diseases].
    Badalian LO.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979 Jun 24; 79(3):257-61. PubMed ID: 571656
    [No Abstract] [Full Text] [Related]

  • 20. A practical approach to molecular diagnostic testing in neuromuscular diseases.
    Arnold WD, Flanigan KM.
    Phys Med Rehabil Clin N Am; 2012 Aug 24; 23(3):589-608. PubMed ID: 22938877
    [Abstract] [Full Text] [Related]

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