These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 21484199)

  • 1. A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.
    Pagnamenta AT; Holt R; Yusuf M; Pinto D; Wing K; Betancur C; Scherer SW; Volpi EV; Monaco AP
    J Neurodev Disord; 2011 Jun; 3(2):124-31. PubMed ID: 21484199
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies.
    Hoffman EP
    Acta Myol; 2020 Dec; 39(4):179-186. PubMed ID: 33458572
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patients.
    Uwineza A; Hitayezu J; Murorunkwere S; Ndinkabandi J; Kalala Malu CK; Caberg JH; Dideberg V; Bours V; Mutesa L
    J Trop Pediatr; 2014 Apr; 60(2):112-7. PubMed ID: 24213305
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort.
    Vengalil S; Preethish-Kumar V; Polavarapu K; Mahadevappa M; Sekar D; Purushottam M; Thomas PT; Nashi S; Nalini A
    J Clin Neurol; 2017 Jan; 13(1):91-97. PubMed ID: 28079318
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. 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]  

  • 9. Phenotype predictions for exon deletions/duplications: A user guide for professionals and clinicians using Becker and Duchenne muscular dystrophy as examples.
    Aartsma-Rus A; den Dunnen JT
    Hum Mutat; 2019 Oct; 40(10):1630-1633. PubMed ID: 31356707
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials.
    Anthony K; Cirak S; Torelli S; Tasca G; Feng L; Arechavala-Gomeza V; Armaroli A; Guglieri M; Straathof CS; Verschuuren JJ; Aartsma-Rus A; Helderman-van den Enden P; Bushby K; Straub V; Sewry C; Ferlini A; Ricci E; Morgan JE; Muntoni F
    Brain; 2011 Dec; 134(Pt 12):3547-59. PubMed ID: 22102647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
    del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM
    Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Unexpected discovery of a fetus with DMD gene deletion using single nucleotide polymorphism array].
    Lin S; Zhou Y; Zhou B; Gu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):563-566. PubMed ID: 28777860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotypic Characterization of a Family With An In-frame Deletion in the DMD Gene and Variable Penetrance.
    Perez-Sanchez I; Sabater-Molina M; Rocamora MEN; Glover G; Escudero F; de Mingo Casado P; Gimeno-Blanes JR
    Curr Gene Ther; 2018; 18(4):246-251. PubMed ID: 29984652
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45-55 Skipping Accompanied by Rescue of Dystrophin Expression.
    Lee JJA; Saito T; Duddy W; Takeda S; Yokota T
    Methods Mol Biol; 2018; 1828():141-150. PubMed ID: 30171539
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study.
    Ansar Z; Nasir A; Moatter T; Khan S; Kirmani S; Ibrahim S; Imam K; Ather A; Samreen A; Hasan Z
    Genet Test Mol Biomarkers; 2019 Jul; 23(7):468-472. PubMed ID: 31157985
    [No Abstract]   [Full Text] [Related]  

  • 16. Deletion mutations in Duchenne muscular dystrophy (DMD) in Western Saudi children.
    Tayeb MT
    Saudi J Biol Sci; 2010 Jul; 17(3):237-40. PubMed ID: 23961084
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community.
    Elhawary NA; Jiffri EH; Jambi S; Mufti AH; Dannoun A; Kordi H; Khogeer A; Jiffri OH; Elhawary AN; Tayeb MT
    Hum Genomics; 2018 Apr; 12(1):18. PubMed ID: 29631625
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A symptomatic male carrier of Duchenne muscular dystrophy with Klinefelter's syndrome mimicking Becker muscular dystrophy.
    Takizawa H; Mori-Yoshimura M; Minami N; Murakami N; Yatabe K; Taira K; Hashimoto Y; Aoki Y; Nishino I; Takahashi Y
    Neuromuscul Disord; 2021 Jul; 31(7):666-672. PubMed ID: 34172357
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies.
    Stockley TL; Akber S; Bulgin N; Ray PN
    Genet Test; 2006; 10(4):229-43. PubMed ID: 17253928
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mutation analysis of 81 cases with Duchenne/Becker muscular dystrophy].
    Li S; Bai Y; Zhao Z; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):762-767. PubMed ID: 27984601
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.