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Journal Abstract Search

120 related items for PubMed ID: 7561572

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  • 4. 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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  • 5. [Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan].
    Odinokova ON, Puzyrev VP, Radzhabaliev ShF, Rakhmonov RA.
    Genetika; 1996 Oct; 32(10):1392-5. PubMed ID: 9091412
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  • 7. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
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  • 8. [Analysis of deletion mutations of the dystrophin gene by the multiplex polymerase chain reaction method in the diagnosis of Duchenne muscular dystrophy].
    Baranov Vs, Gorbunova VN, Malysheva OV, Krasil'nikov VV.
    Mol Gen Mikrobiol Virusol; 1991 Sep 15; (9):13-5. PubMed ID: 1745268
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  • 9. Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion "hot spot" region.
    Coral-Vazquez R, Arenas D, Cisneros B, Peñaloza L, Salamanca F, Kofman S, Mercado R, Montañez C.
    Am J Med Genet; 1997 Jun 13; 70(3):240-6. PubMed ID: 9188659
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  • 10. Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.
    Hallwirth Pillay KD, Bill PL, Madurai S, Mubaiwa L, Rapiti P.
    J Neurol Sci; 2007 Jan 15; 252(1):1-3. PubMed ID: 17141273
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  • 11. [Detection of extensive deletions and duplications in the dystrophin gene].
    Fajkusová L, Kuhrová V, Hájek J, Fajkus J.
    Cas Lek Cesk; 1997 Mar 12; 136(5):148-50. PubMed ID: 9221188
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  • 12. PGD for dystrophin gene deletions using fluorescence in situ hybridization.
    Malmgren H, White I, Johansson S, Levkov L, Iwarsson E, Fridström M, Blennow E.
    Mol Hum Reprod; 2006 May 12; 12(5):353-6. PubMed ID: 16608904
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  • 13. Detection of gene deletions by PCR analysis in a Malaysian patient with Duchenne muscular dystrophy.
    Lee MK, Manonmani V, Arahata K.
    Med J Malaysia; 1993 Mar 12; 48(1):46-50. PubMed ID: 8341171
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  • 14. Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.
    Kitoh Y, Matsuo M, Nishio H, Nakamura H.
    Kobe J Med Sci; 1994 Apr 12; 40(2):39-48. PubMed ID: 7823533
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  • 15. 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 12; 39(4):367-72. PubMed ID: 16413013
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  • 17. 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 12; 21(1):151-6. PubMed ID: 9225508
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  • 19. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
    Tuffery-Giraud S, Chambert S, Demaille J, Claustres M.
    Ann Biol Clin (Paris); 1999 Jun 12; 57(4):417-26. PubMed ID: 10432364
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