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Journal Abstract Search

276 related items for PubMed ID: 2879923

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  • 2. 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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  • 4. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
    Thompson MW, Ray PN, Belfall B, Duff C, Logan C, Oss I, Worton RG.
    J Med Genet; 1986 Dec; 23(6):548-55. PubMed ID: 2879926
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  • 6. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
    Ubagai T, Katayama S.
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):211-27. PubMed ID: 1684391
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  • 7. DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.
    Soong BW, Tsai TF, Su CH, Kao KP, Hsiao KJ, Su TS.
    Am J Med Genet; 1991 Mar 15; 38(4):593-600. PubMed ID: 1676564
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  • 8. Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene.
    Zeng YT, Chen MJ, Ren ZR, Qui XK, Huang SZ.
    J Med Genet; 1991 Mar 15; 28(3):167-70. PubMed ID: 1675685
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  • 13. 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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  • 15. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF, Harris SG, Tsao CC, Ward PA, Caskey CT.
    Neurology; 1986 Dec 07; 36(12):1553-62. PubMed ID: 2878392
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  • 16. Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.
    Lindlöf M, Kääriäinen H, van Ommen GJ, de la Chapelle A.
    Clin Genet; 1988 Feb 07; 33(2):131-9. PubMed ID: 3162851
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  • 17. Molecular deletion patterns in Duchenne and Becker type muscular dystrophy.
    Liechti-Gallati S, Koenig M, Kunkel LM, Frey D, Boltshauser E, Schneider V, Braga S, Moser H.
    Hum Genet; 1989 Mar 07; 81(4):343-8. PubMed ID: 2784778
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  • 18. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
    Monaco AP, Bertelson CJ, Colletti-Feener C, Kunkel LM.
    Hum Genet; 1987 Mar 07; 75(3):221-7. PubMed ID: 2881877
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