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Journal Abstract Search

223 related items for PubMed ID: 31207536

  • 1. 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; 240():15-22. PubMed ID: 31207536
    [Abstract] [Full Text] [Related]

  • 2. Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing.
    Chen M, Chen C, Huang X, Sun J, Jiang L, Li Y, Zhu Y, Tian C, Li Y, Lu Z, Wang Y, Zeng F, Yang Y, Song X, Peng Z, Yin C, Chen D.
    Prenat Diagn; 2020 Jul; 40(8):918-924. PubMed ID: 31916613
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 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 14; 48(3):161-4. PubMed ID: 23849935
    [Abstract] [Full Text] [Related]

  • 5. Noninvasive prenatal diagnosis of duchenne muscular dystrophy in five Chinese families based on relative mutation dosage approach.
    Zhao G, Wang X, Liu L, Dai P, Kong X.
    BMC Med Genomics; 2021 Nov 22; 14(1):275. PubMed ID: 34802424
    [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. Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma.
    Xu Y, Li X, Ge HJ, Xiao B, Zhang YY, Ying XM, Pan XY, Wang L, Xie WW, Ni L, Chen SP, Jiang WT, Liu P, Ye H, Cao Y, Zhang JM, Liu Y, Yang ZJ, Chen YW, Chen F, Jiang H, Ji X.
    Genet Med; 2015 Nov 25; 17(11):889-96. PubMed ID: 25654318
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Haplotype-Based Noninvasive Prenatal Diagnosis of 21 Families With Duchenne Muscular Dystrophy: Real-World Clinical Data in China.
    Kong L, Li S, Zhao Z, Feng J, Chen G, Liu L, Tang W, Li S, Li F, Han X, Wu D, Zhang H, Sun L, Kong X.
    Front Genet; 2021 Apr 05; 12():791856. PubMed ID: 34970304
    [Abstract] [Full Text] [Related]

  • 10. [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]

  • 11. [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]

  • 12. Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus.
    Yoo SK, Lim BC, Byeun J, Hwang H, Kim KJ, Hwang YS, Lee J, Park JS, Lee YS, Namkung J, Park J, Lee S, Shin JY, Seo JS, Kim JI, Chae JH.
    Clin Chem; 2015 Jun 10; 61(6):829-37. PubMed ID: 25847990
    [Abstract] [Full Text] [Related]

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  • 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 10; 52(4):534-9. PubMed ID: 24411039
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  • 16. [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]

  • 17. Noninvasive prenatal testing of Duchenne muscular dystrophy in a twin gestation.
    Kong L, Li S, Zhao Z, Feng J, Liu L, Tang W, Zhang H, Wu D, Sun L, Kong X.
    Prenat Diagn; 2022 Apr 10; 42(4):518-523. PubMed ID: 35220584
    [Abstract] [Full Text] [Related]

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  • 19. Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis.
    Jang SS, Lim BC, Yoo SK, Shin JY, Kim KJ, Seo JS, Kim JI, Chae JH.
    Sci Rep; 2018 Jun 06; 8(1):8678. PubMed ID: 29875376
    [Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of de novo DMD duplication by multiplex ligation-dependent probe amplification (MLPA) after noninvasive prenatal screening (NIPS) at 11 gestational weeks.
    Kim SH, Hong SY, Lee MJ, Kang KM, Park JE, Shim SH, Cha DH.
    Taiwan J Obstet Gynecol; 2021 May 06; 60(3):570-573. PubMed ID: 33966752
    [Abstract] [Full Text] [Related]

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