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Journal Abstract Search

220 related items for PubMed ID: 8588583

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  • 2. Diagnosis and carrier detection in a Duchenne muscular dystrophy family by multiplex polymerase chain reaction and microsatellite analysis.
    Jongpiputvanich S, Norapucsunton T, Mutirangura A.
    J Med Assoc Thai; 1996 Dec; 79 Suppl 1():S15-21. PubMed ID: 9071063
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  • 4. Usefulness of dinucleotide polymorphism markers in genetic analysis of Duchenne's muscular dystrophy cases in Singapore.
    Lai PS, Chiu LL, Low PS, Lee WL, Tay JS.
    Southeast Asian J Trop Med Public Health; 1995 Dec; 26 Suppl 1():175-8. PubMed ID: 8629101
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  • 5. [Carrier genetic diagnosis of intron and/or exon-deletion Duchenne muscular dystrophy by microsatellite analysis and quantitative polymerase chain reaction].
    Huang W, Zhang C, Xie YM, Chen SL, Zhang WX, Yao XL, Zeng Y, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):72-5. PubMed ID: 17285549
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  • 8. [Rapid screening of the Duchenne muscular dystrophy gene deletion by two multiplex PCR].
    Ma S.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Feb; 15(1):74-8. PubMed ID: 8324844
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  • 10. Detection of DMD gene deletions in Thai children patients.
    Kamolsilp M, Paditaporn R, Noonai A, Wasant P.
    Southeast Asian J Trop Med Public Health; 1995 Feb; 26 Suppl 1():172-4. PubMed ID: 8629100
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  • 12. Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection.
    Prior TW, Papp AC, Snyder PJ, Sedra MS, Western LM, Bartolo C, Moxley RT, Mendell JR.
    Am J Med Genet; 1994 Mar 01; 50(1):68-73. PubMed ID: 8160755
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  • 16. Gene deletion and carrier detection in the family of Becker muscular dystrophy by short tandem repeat sequence polymorphism.
    Cai S, Shen D, Wang J.
    Chin Med J (Engl); 1999 Mar 01; 112(3):242-5. PubMed ID: 11593558
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  • 17. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
    Pikó H, Vancsó V, Nagy B, Bán Z, Herczegfalvi A, Karcagi V.
    Neuromuscul Disord; 2009 Feb 01; 19(2):108-12. PubMed ID: 19084397
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