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Journal Abstract Search

130 related items for PubMed ID: 2564816

  • 1. 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]

  • 2. Molecular probe protocol for determining carrier status in Duchenne and Becker muscular dystrophies.
    Prior TW, Friedman KJ, Highsmith WE, Perry TR, Silverman LM.
    Clin Chem; 1990 Mar; 36(3):441-5. PubMed ID: 1968788
    [Abstract] [Full Text] [Related]

  • 3. Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studies.
    Prior TW, Blasco PA, Dove JL, Leshner RT, Gruemer HD.
    Clin Chem; 1989 Apr; 35(4):679-83. PubMed ID: 2564818
    [Abstract] [Full Text] [Related]

  • 4. The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.
    Laing NG, Mears ME, Chandler DC, Layton MG, Thomas HE, Johnsen RD, Goldblatt J, Kakulas BA.
    Med J Aust; 1991 Jan 07; 154(1):14-8. PubMed ID: 1670611
    [Abstract] [Full Text] [Related]

  • 5. Molecular biological approaches to genetic disorders in prenatal diagnosis.
    Katayama S.
    Early Hum Dev; 1992 Jan 07; 29(1-3):149-53. PubMed ID: 1356752
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.
    Chen JD, Denton MJ, Serravalle S, Morgan G.
    Aust Paediatr J; 1988 Dec 07; 24(6):351-3. PubMed ID: 2907402
    [Abstract] [Full Text] [Related]

  • 7. Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms.
    Laing NG, Walker AP, Akkari PA, Chandler DC, Layton MG, Mears ME, Yamada T, Bartlett RJ, Pericak-Vance MA, Hung WY.
    Prenat Diagn; 1991 Jan 07; 11(1):63-7. PubMed ID: 1709287
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.
    Old JM, Davies KE.
    J Med Genet; 1986 Dec 07; 23(6):556-9. PubMed ID: 2879927
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes.
    Katayama S, Montano M, Slotnick RN, Lebo RV, Golbus MS.
    Am J Obstet Gynecol; 1988 Mar 07; 158(3 Pt 1):548-55. PubMed ID: 2894769
    [Abstract] [Full Text] [Related]

  • 10. Carrier detection and gene analysis of Duchenne muscular dystrophy.
    Pearson PL, van Ommen GJ, Bakker E.
    Cold Spring Harb Symp Quant Biol; 1986 Mar 07; 51 Pt 1():353-8. PubMed ID: 2884063
    [No Abstract] [Full Text] [Related]

  • 11. Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy.
    Roberts RG, Cole CG, Hart KA, Bobrow M, Bentley DR.
    Nucleic Acids Res; 1989 Jan 25; 17(2):811. PubMed ID: 2563578
    [No Abstract] [Full Text] [Related]

  • 12. Molecular deletion analysis in Duchenne muscular dystrophy.
    Thomas NS, Ray PN, Worton RG, Harper PS.
    J Med Genet; 1986 Dec 25; 23(6):509-15. PubMed ID: 2879923
    [Abstract] [Full Text] [Related]

  • 13. Detection of Duchenne/Becker muscular dystrophy carriers by densitometric scanning.
    Prior TW, Friedman KJ, Silverman LM.
    Clin Chem; 1989 Jun 25; 35(6):1256-7. PubMed ID: 2731350
    [No Abstract] [Full Text] [Related]

  • 14. Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
    Kääriäinen H, Lindlöf M, Somer H, de la Chapelle A.
    Clin Genet; 1990 Mar 25; 37(3):179-87. PubMed ID: 1969777
    [Abstract] [Full Text] [Related]

  • 15. Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy.
    Hyser CL, Griggs RC, Mendell JR, Polakowska R, Quirk S, Brooke MH, Fenichel GM, Doherty RA.
    Neurology; 1987 Jan 25; 37(1):4-10. PubMed ID: 2879259
    [Abstract] [Full Text] [Related]

  • 16. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
    Lindlöf M, Kääriäinen H, Davies KE, de la Chapelle A.
    J Med Genet; 1986 Dec 25; 23(6):560-72. PubMed ID: 2879928
    [Abstract] [Full Text] [Related]

  • 17. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL.
    J Med Genet; 1986 Dec 25; 23(6):573-80. PubMed ID: 2879929
    [Abstract] [Full Text] [Related]

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  • 20. DNA probes in Duchenne muscular dystrophy.
    Clayton J, Emery A.
    Lancet; 1984 Nov 17; 2(8412):1151-2. PubMed ID: 6150202
    [No Abstract] [Full Text] [Related]

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