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Journal Abstract Search

425 related items for PubMed ID: 2879928

  • 1. 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; 23(6):560-72. PubMed ID: 2879928
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  • 3. 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; 24(6):351-3. PubMed ID: 2907402
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  • 6. 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
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  • 7. 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; 158(3 Pt 1):548-55. PubMed ID: 2894769
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  • 9. 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
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  • 10. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
    Meredith AL, Huson SM, Lunt PW, Sarfarazi M, Harley HG, Brook JD, Shaw DJ, Harper PS.
    Br Med J (Clin Res Ed); 1986 Nov 22; 293(6558):1353-6. PubMed ID: 2878705
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  • 12. 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 22; 37(1):4-10. PubMed ID: 2879259
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  • 13. Molecular analysis of 25 Chinese families with Duchenne/Becker muscular dystrophy.
    Ko TM, Chen CF, Chiu HC, Hsieh FJ, Lee TY.
    J Formos Med Assoc; 1990 Oct 22; 89(10):850-6. PubMed ID: 1981771
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  • 14. Linkage studies in Duchenne and Becker muscular dystrophies.
    Walker A, Hart K, Cole C, Hodgson S, Johnson L, Dubowitz V, Bobrow M.
    J Med Genet; 1986 Dec 22; 23(6):538-47. PubMed ID: 2879925
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  • 15. The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
    Hodgson S, Walker A, Cole C, Hart K, Johnson L, Heckmatt J, Dubowitz V, Bobrow M.
    J Med Genet; 1987 Mar 22; 24(3):152-9. PubMed ID: 3572997
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  • 18. [Carrier diagnosis and prenatal prognosis using DNA analysis in X-chromosome-linked Duchenne and Becker muscular dystrophy].
    Moser H, Liechti-Gallati S, Braga S, Hirsiger H.
    Schweiz Med Wochenschr; 1987 Dec 19; 117(51):2061-73. PubMed ID: 3433090
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