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Journal Abstract Search


202 related items for PubMed ID: 28181689

  • 1. Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.
    Wang H, Xu Y, Liu X, Wang L, Jiang W, Xiao B, Wei W, Chen Y, Ye W, Ji X.
    Prenat Diagn; 2017 Apr; 37(4):356-364. PubMed ID: 28181689
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [Clinical value of MLPA in the prenatal gene diagnosis of Duchenne muscular dystrophy].
    Li Q, Li SY, Zhang HM, He WZ, Ma XY, Wang XM, Xian JJ, Sun XF, Chen DJ, Yu YH.
    Zhonghua Fu Chan Ke Za Zhi; 2013 Mar 14; 48(3):161-4. PubMed ID: 23849935
    [Abstract] [Full Text] [Related]

  • 4. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
    Zhao W, Jiang N, Li S, Li JS, Miao Y, Liang SY, Yu DY.
    Zhonghua Fu Chan Ke Za Zhi; 2019 Apr 25; 54(4):226-231. PubMed ID: 31006187
    [Abstract] [Full Text] [Related]

  • 5. [Mutation analysis and prenatal diagnosis of families affected with Duchenne and Becker muscular dystrophy].
    Wang WJ, Zhu HY, Zhu RF, Yang Y, Zhu XY, Duan HL, Zhang Y, Wu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb 25; 30(1):45-8. PubMed ID: 23450478
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  • 7. [Mutation analysis and prenatal diagnosis for 50 pedigrees affected with Duchenne/Becker muscular dystrophy].
    Li H, Xu C, Mao Y, Lu J, Xiang Y, Xu X, Tang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):169-174. PubMed ID: 29652985
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  • 9. Rapid method for targeted prenatal diagnosis of Duchenne muscular dystrophy in Vietnam.
    Ta MH, Tran TH, Do NH, Pham le AT, Bui TH, Ta VT, Tran VK.
    Taiwan J Obstet Gynecol; 2013 Dec 10; 52(4):534-9. PubMed ID: 24411039
    [Abstract] [Full Text] [Related]

  • 10. Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination.
    Percesepe A, Ferrari M, Coviello D, Zanussi M, Castagni M, Neri I, Travi M, Forabosco A, Tedeschi S.
    Prenat Diagn; 2005 Nov 10; 25(11):1011-4. PubMed ID: 16231306
    [Abstract] [Full Text] [Related]

  • 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 10; 26(3):318-22. PubMed ID: 19504448
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  • 13. [Genetic analysis and reproductive intervention of 7 families with gonadal mosaicism for Duchenne muscular dystrophy].
    Gao B, Yang X, Hu X, He W, Zhao X, Gong F, Du J, Zhang Q, Lu G, Lin G, Li W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Apr 10; 40(4):423-428. PubMed ID: 36972936
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  • 15. Development of a comprehensive real-time PCR assay for dystrophin gene analysis and prenatal diagnosis of Chinese families.
    Zhang T, Liu S, Wei T, Yong J, Mao Y, Lu X, Xie J, Ke Q, Jin F, Qi M.
    Clin Chim Acta; 2013 Sep 23; 424():33-8. PubMed ID: 23680072
    [Abstract] [Full Text] [Related]

  • 16. [Efficiency of multiplex ligation-dependent probe amplification combined with short tandem repeat linkage analysis for the prenatal diagnosis for Duchenne muscular dystrophy].
    Li T, Wu D, Hou QF, Wang L, Guo QN, Kang B, Liu HY, Yang K, Ding XB, Liao SX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb 23; 30(1):40-4. PubMed ID: 23450477
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  • 18. [Germinal mosaicism for partial deletion of the Dystrophin gene in a family affected with Duchenne muscular dystrophy].
    Xiao H, Zhang Z, Li T, Zhang Q, Guo Q, Wu D, Wang H, Zhang M, Gao Y, Liao S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct 10; 36(10):1015-1018. PubMed ID: 31598949
    [Abstract] [Full Text] [Related]

  • 19. Gene diagnosis for nine Chinese patients with DMD/BMD by multiplex ligation-dependent probe amplification and prenatal diagnosis for one of them.
    Wu Y, Yin G, Fu K, Wu D, Zhai Q, Du H, Huang Z, Niu Y.
    J Clin Lab Anal; 2009 Oct 10; 23(6):380-6. PubMed ID: 19927354
    [Abstract] [Full Text] [Related]

  • 20. DMD/BMD prenatal diagnosis and treatment expectation in a single centre in China for 15 years.
    Zhong X, Cui S, Liu L, Yang Y, Kong X.
    BMC Med Genomics; 2021 Jul 08; 14(1):181. PubMed ID: 34238289
    [Abstract] [Full Text] [Related]


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