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Journal Abstract Search

63 related items for PubMed ID: 9798335

  • 1.
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  • 3. Quantitative ELISA for platelet m-calpain: a phenotypic index for detection of carriers of Duchenne muscular dystrophy.
    Hussain T, Kumar DV, Sundaram C, Mohandas S, Anandaraj MP.
    Clin Chim Acta; 1998 Jan 12; 269(1):13-20. PubMed ID: 9498100
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  • 4. A quantitative polymerase chain reaction (PCR) assay completely discriminates between Duchenne and Becker muscular dystrophy deletion carriers and normal females.
    Pastore L, Caporaso MG, Frisso G, Orsini A, Santoro L, Sacchetti L, Salvatore F.
    Mol Cell Probes; 1996 Apr 12; 10(2):129-37. PubMed ID: 8737397
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  • 6. 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 12; 79 Suppl 1():S15-21. PubMed ID: 9071063
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  • 7. Calcium activated neutral protease in blood cells from patients & carriers of Duchenne muscular dystrophy.
    Moses L, Shailaja B, Anandaraj MP.
    Indian J Med Res; 1990 Feb 12; 92():5-8. PubMed ID: 2347611
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  • 8. 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 12; 36(3):211-27. PubMed ID: 1684391
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  • 9. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S, Shukin RJ, McGillivray BC, Ray PN, Worton RG.
    Am J Med Genet; 1988 Feb 12; 29(2):419-23. PubMed ID: 2895584
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  • 11. Detection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction.
    Sinha S, Pradhan S, Mittal RD, Mittal B.
    Indian J Med Res; 1992 Oct 12; 96():297-301. PubMed ID: 1459673
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  • 12. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug 12; 23(4):231-3, 255. PubMed ID: 1979269
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  • 13. [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 12; 24(1):72-5. PubMed ID: 17285549
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  • 14. Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals: deletion detection and familial diagnosis.
    Patiño A, Narbona J, García-Delgado M.
    Am J Med Genet; 1995 Nov 06; 59(2):182-7. PubMed ID: 8588583
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  • 15. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N.
    Am J Med Genet; 1989 Dec 06; 34(4):555-61. PubMed ID: 2576185
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  • 16. Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometry.
    Laing NG, Siddique T, Bartlett R, Yamaoka LH, Hung WY, Pericak-Vance MA, Roses AD.
    Clin Genet; 1989 Jun 06; 35(6):393-8. PubMed ID: 2736788
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  • 17. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW, Papp AC, Snyder PJ, Mendell JR.
    Muscle Nerve; 1992 Aug 06; 15(8):960-3. PubMed ID: 1353862
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  • 18. Comparison of serum creatine kinase estimation with short tandem repeats based linkage analysis in carriers and affected children of Duchenne muscular dystrophy.
    Hashim R, Shaheen S, Ahmad S, Sattar A, Khan FA.
    J Ayub Med Coll Abbottabad; 2011 Aug 06; 23(1):125-8. PubMed ID: 22830166
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  • 20. Deletion analysis of Duchenne muscular dystrophy using cDNA probes and multiplex PCR.
    Radosavljević D, Todorović D, Crkvenjakov R.
    Neurol Croat; 1991 Aug 06; 40(3):157-64. PubMed ID: 1681950
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