BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

421 related articles for article (PubMed ID: 31379145)

  • 1. Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene.
    Yang YM; Yan K; Liu B; Chen M; Wang LY; Huang YZ; Qian YQ; Sun YX; Li HG; Dong MY
    J Zhejiang Univ Sci B; 2019 Sept.; 20(9):753-765. PubMed ID: 31379145
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy].
    Bai Y; Li S; Zong YN; Li XL; Zhao ZH; Kong XD
    Zhonghua Yi Xue Za Zhi; 2016 Apr; 96(16):1261-9. PubMed ID: 27122458
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hybrid minigene splicing assay verified the pathogenicity of a novel splice site variant in the dystrophin gene of a Chinese patient with typical Duchenne muscular dystrophy phenotype.
    Wang Z; Lin Y; Qiu L; Zheng D; Yan A; Zeng J; Lan F
    Clin Chem Lab Med; 2016 Sep; 54(9):1435-40. PubMed ID: 26985686
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 20(1):139. PubMed ID: 31412794
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 54(4):226-231. PubMed ID: 31006187
    [No Abstract]   [Full Text] [Related]  

  • 6. NGS-based targeted sequencing identified six novel variants in patients with Duchenne/Becker muscular dystrophy from southwestern China.
    Tang F; Xiao Y; Zhou C; Zhang H; Wang J; Zeng Y
    BMC Med Genomics; 2023 May; 16(1):121. PubMed ID: 37254189
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 20(1):180. PubMed ID: 31727011
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Targeted sequencing of the
    Aravind S; Ashley B; Mannan A; Ganapathy A; Ramesh K; Ramachandran A; Nongthomba U; Shastry A
    Indian J Med Res; 2019 Sep; 150(3):282-289. PubMed ID: 31719299
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 131(7):770-775. PubMed ID: 29578119
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 61(6):483-9. PubMed ID: 26911353
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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; 39(9):925-931. PubMed ID: 36082559
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy].
    Zhang YZ; Xiong H; Wang XZ; Wang S; Luo J; Wang JM; Jiang YW; Chang XZ; Pan H; Qi JG; Li WZ; Yuan Y; Wu XR
    Beijing Da Xue Xue Bao Yi Xue Ban; 2010 Dec; 42(6):661-6. PubMed ID: 21170096
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients.
    Lee T; Takeshima Y; Kusunoki N; Awano H; Yagi M; Matsuo M; Iijima K
    J Hum Genet; 2014 Jan; 59(1):46-50. PubMed ID: 24225992
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic profile of Brazilian patients with dystrophinopathies.
    de Almeida PAD; Machado-Costa MC; Manzoli GN; Ferreira LS; Rodrigues MCS; Bueno LSM; Saute JAM; Pinto Vairo F; Matte US; Siebert M; Cossio SL; Macedo GS; Winckler PB; Becker MM; Magalhães LVB; Gonçalves MVM; Marrone CD; Nucci A; França MC
    Clin Genet; 2017 Aug; 92(2):199-203. PubMed ID: 28116794
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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
    [TBL] [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; 31(3):338-43. PubMed ID: 24928015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy.
    Zimowski JG; Massalska D; Holding M; Jadczak S; Fidziańska E; Lusakowska A; Kostera-Pruszczyk A; Kamińska A; Zaremba J
    Neurol Neurochir Pol; 2014; 48(6):416-22. PubMed ID: 25482253
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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; 22(6):602-607. PubMed ID: 32571459
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.
    Todorova A; Todorov T; Georgieva B; Lukova M; Guergueltcheva V; Kremensky I; Mitev V
    Neuromuscul Disord; 2008 Aug; 18(8):667-70. PubMed ID: 18653336
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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; 30(1):45-8. PubMed ID: 23450478
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.