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Journal Abstract Search

119 related items for PubMed ID: 15300642

  • 1. [Single cell analysis of some deletion in dystrophin gene exons and gender determination by 3-plex nested PCR].
    Huang W, Zhang C, Xie YM, Chen SL, Jiao ZX, Zhou CQ, Zhang WX, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):389-91. PubMed ID: 15300642
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  • 2. [Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR].
    Wu YL, Wu LQ, Li YP, Liu DE, Zeng Q, Zhu HY, Pan Q, Liang DS, Hu H, Long ZG, Li J, Dai HP, Xia K, Xia JH.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):246-51. PubMed ID: 17478931
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  • 3. 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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  • 9. Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).
    Lai KK, Lo IF, Tong TM, Cheng LY, Lam ST.
    Clin Biochem; 2006 Apr; 39(4):367-72. PubMed ID: 16413013
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  • 10. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
    Sertić J, Barisić N, Sostarko M, Brzović Z, Stavljenić-Rukavina A.
    Coll Antropol; 1997 Jun; 21(1):151-6. PubMed ID: 9225508
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  • 13. Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophy.
    Malcov M, Schwartz T, Mei-Raz N, Yosef DB, Amit A, Lessing JB, Shomrat R, Orr-Urtreger A, Yaron Y.
    Fetal Diagn Ther; 2004 Jun; 19(2):199-206. PubMed ID: 14764971
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  • 17. Rapid identification of female carriers of DMD/BMD by quantitative real-time PCR.
    Joncourt F, Neuhaus B, Jostarndt-Foegen K, Kleinle S, Steiner B, Gallati S.
    Hum Mutat; 2004 Apr; 23(4):385-91. PubMed ID: 15024733
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  • 18. [Identification of disease-causing point mutations in DMD patients' dystrophin gene without large deletions/duplications].
    Shen BC, Zhang C, Chen SL, Sun XF, Li SY, Yao XL, Wang SH, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):392-6. PubMed ID: 16883524
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  • 19. Allele-specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy.
    Moutou C, Gardes N, Rongières C, Ohl J, Bettahar-Lebugle K, Wittemer C, Gerlinger P, Viville S.
    Prenat Diagn; 2001 Jun; 21(6):498-503. PubMed ID: 11438957
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  • 20. Cloning and sequencing of junction fragment with exons 45-54 deletion of dystrophin gene.
    Zhong M, Pan SY, Lu BX, Li W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):138-41. PubMed ID: 16604481
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