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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

471 related items for PubMed ID: 9225508

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  • 2. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
    Li H, Ding J, Wang W, Chen Y, Lu W, Shao H, Wu BL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
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  • 4. 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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  • 5. [Gene deletion analysis in molecular diagnosis of Duchenne-Becker muscular dystrophy].
    Endreffy E, László A, Kálmán M, Krenács T, Raskó I.
    Orv Hetil; 1994 Feb 20; 135(8):399-403. PubMed ID: 8139842
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  • 7. 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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  • 12. [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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  • 13. Comparative study on deletions of the dystrophin gene in three Asian populations.
    Lai PS, Takeshima Y, Adachi K, Van Tran K, Nguyen HT, Low PS, Matsuo M.
    J Hum Genet; 2002 Mar 12; 47(10):552-5. PubMed ID: 12376747
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  • 19. 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 12; 51(2):223-6. PubMed ID: 14571009
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