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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

269 related items for PubMed ID: 37254189

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  • 3. Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy.
    Kong X, Zhong X, Liu L, Cui S, Yang Y, Kong L.
    BMC Med Genet; 2019 Aug 14; 20(1):139. PubMed ID: 31412794
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  • 4. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
    Zhang J, Ma D, Liu G, Wang Y, Liu A, Li L, Luo C, Hu P, Xu Z.
    BMC Med Genet; 2019 Nov 14; 20(1):180. PubMed ID: 31727011
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  • 9. Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.
    Okubo M, Minami N, Goto K, Goto Y, Noguchi S, Mitsuhashi S, Nishino I.
    J Hum Genet; 2016 Jun 14; 61(6):483-9. PubMed ID: 26911353
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  • 11. [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 14; 26(3):318-22. PubMed ID: 19504448
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  • 12. [Variant analysis and therapeutic prospect for Chinese pedigrees affected with Duchenne/Becker muscular dystrophy from a single center over the past 15 years].
    Zhong X, Liu L, Kong X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 May 10; 38(5):425-429. PubMed ID: 33974248
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  • 16. [A predictive analysis of the association between clinical phenotypes and genotypes in children with Becker muscular dystrophy/Duchenne muscular dystrophy].
    Niu HH, Tao DY, Cheng SQ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2020 Jun 10; 22(6):602-607. PubMed ID: 32571459
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  • 20. Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.
    Zhong J, Xu T, Chen G, Liao H, Zhang J, Lan D.
    Muscle Nerve; 2017 Jul 10; 56(1):117-121. PubMed ID: 27750387
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