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Journal Abstract Search

118 related items for PubMed ID: 35810418

  • 1. [Analysis of results of prenatal diagnosis for 67 pedigrees affected with Duchenne muscular dystrophy in the central plain region of China].
    Gao Z, Liu L, Wang Y, Wang Y, Huang W, Kong X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jul 10; 39(7):669-673. PubMed ID: 35810418
    [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. [Genetic testing and prenatal diagnosis of 671 Chinese pedigrees affected with Duchenne/Becker muscular dystrophy].
    Luo S, He W, Zhao X, Yang X, Gao B, Li S, Du J, Zhang Q, Tan Y, Lu G, Lin G, Li W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Sep 10; 39(9):925-931. PubMed ID: 36082559
    [Abstract] [Full Text] [Related]

  • 4. [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 10; 48(3):161-4. PubMed ID: 23849935
    [Abstract] [Full Text] [Related]

  • 5. Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China.
    Zhao HH, Sun XP, Shi MC, Yi YX, Cheng H, Wang XX, Xu QC, Ma HM, Wu HQ, Jin QW, Niu Q.
    Chin Med J (Engl); 2018 Apr 05; 131(7):770-775. PubMed ID: 29578119
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. [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
    [Abstract] [Full Text] [Related]

  • 9. [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 10; 30(1):45-8. PubMed ID: 23450478
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. [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
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of 1408 foetuses at risk of DMD/BMD by MLPA and Sanger sequencing combined with STR linkage analysis.
    Hua C, Liu L, Kong X.
    BMC Med Genomics; 2023 Dec 01; 16(1):310. PubMed ID: 38041114
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 37(4):356-364. PubMed ID: 28181689
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 52(4):534-9. PubMed ID: 24411039
    [Abstract] [Full Text] [Related]

  • 15. Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.
    Chen M, Chen C, Li Y, Yuan Y, Lai Z, Guo F, Wang Y, Huang X, Li S, Wu R, Peng Z, Sun J, Chen D.
    Eur J Obstet Gynecol Reprod Biol; 2019 Sep 01; 240():15-22. PubMed ID: 31207536
    [Abstract] [Full Text] [Related]

  • 16. [Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].
    Zhang Y, Liu X, He R, Ma H, Zhao Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun 01; 31(3):338-43. PubMed ID: 24928015
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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 Jul 08; 23(6):380-6. PubMed ID: 19927354
    [Abstract] [Full Text] [Related]

  • 19. [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 08; 30(1):40-4. PubMed ID: 23450477
    [Abstract] [Full Text] [Related]

  • 20. [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]

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