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Journal Abstract Search

76 related items for PubMed ID: 22166894

  • 1.
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  • 2. Deletion analysis & calpain status for carrier detection in a family with Duchenne muscular dystrophy.
    Hussain T, Devi NG, Kumari CK, Anandaraj MP.
    Indian J Med Res; 1998 Sep; 108():93-7. PubMed ID: 9798335
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  • 3. 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 Sep; 23(1):125-8. PubMed ID: 22830166
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  • 6. The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis.
    Ferreiro V, Giliberto F, Francipane L, Szijan I.
    Mol Diagn; 2005 Sep; 9(2):67-80. PubMed ID: 16137182
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  • 7. [Carrier detection of Duchenne/Becker muscular dystrophy by analysis of STRs loci linked to the gene of dystrophin in Venezuelan families].
    Delgado-Luengo WN, Borjas-Fuentes L, Zabala-Fernández W, Fernández-Salgado E, Solís-Añez E, Chávez C, Martínez-Basalo C, González-Ferrer S, Rojas-Atencio A, Morales-Machin A, Peña J, Pineda-Bernal L, González R, Miranda LE, Delgado-Luengo J, Hernández ML, Chacín JA, Quintero M.
    Invest Clin; 2002 Dec; 43(4):239-54. PubMed ID: 12520997
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  • 9. Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.
    Malcov M, Ben-Yosef D, Schwartz T, Mey-Raz N, Azem F, Lessing JB, Amit A, Yaron Y.
    Prenat Diagn; 2005 Dec; 25(13):1200-5. PubMed ID: 16353285
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  • 10. Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.
    Zhu HY, Wu LQ, Liang DS, Pan Q, Xia JH.
    Yi Chuan Xue Bao; 2006 Mar; 33(3):206-12. PubMed ID: 16553208
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  • 12. Detection of Duchenne/Becker muscular dystrophy carriers in a group of Iranian families by linkage analysis.
    Malayeri FA, Panjehpour M, Movahedian A, Ghaffarpour M, Zamani GR, Tabrizi MH, Zamani M.
    Acta Med Iran; 2011 Mar; 49(3):142-8. PubMed ID: 21681700
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  • 13. Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification.
    Ren Z, Zeng HT, Xu YW, Zhuang GL, Deng J, Zhang C, Zhou CQ.
    Fertil Steril; 2009 Feb; 91(2):359-64. PubMed ID: 18359022
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  • 14. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
    Ligon AH, Kashork CD, Richards CS, Shaffer LG.
    Eur J Hum Genet; 2000 Apr; 8(4):293-8. PubMed ID: 10854113
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  • 15. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
    Kumari D, Mital A, Gupta M, Goyle S.
    Neurol India; 2003 Jun; 51(2):223-6. PubMed ID: 14571009
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  • 16. Validation and comparison of two quantitative real-time PCR assays for direct detection of DMD/BMD carriers.
    Hayat Nosaeid M, Mahdian R, Jamali S, Maryami F, Babashah S, Maryami F, Karimipoor M, Zeinali S.
    Clin Biochem; 2009 Aug; 42(12):1291-9. PubMed ID: 19439162
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  • 17. DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
    Hofstra RM, Mulder IM, Vossen R, de Koning-Gans PA, Kraak M, Ginjaar IB, van der Hout AH, Bakker E, Buys CH, van Ommen GJ, van Essen AJ, den Dunnen JT.
    Hum Mutat; 2004 Jan; 23(1):57-66. PubMed ID: 14695533
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  • 18.
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  • 19. [Application of PCR technique in genetic diagnosis of Duchenne/Becker muscular dystrophy].
    Liu YM, Feng ZC, Fang ZW.
    Di Yi Jun Yi Da Xue Xue Bao; 2002 Aug; 22(8):731-3. PubMed ID: 12376264
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  • 20. [Carrier detection of Duchenne/Becker muscular dystrophy in Chinese families by microsatellite analysis].
    Huang W, Zhang C, Xie YM, Chen SL, Zhang WX, Lu XL, Yao XL, Zeng Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun; 21(3):224-8. PubMed ID: 15192822
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