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Journal Abstract Search

76 related items for PubMed ID: 22166894

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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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  • 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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  • 8. [Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].
    Zhu HY, Li J, Yang Y, Wu X, Zhu XY, Zhu RF, Zhang Y, Duan HL, Hu YL.
    Zhonghua Yi Xue Za Zhi; 2009 Jul 07; 89(25):1753-6. PubMed ID: 19862979
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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 Jul 07; 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 07; 91(2):359-64. PubMed ID: 18359022
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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 07; 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 07; 23(1):57-66. PubMed ID: 14695533
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