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 *

598 related articles for article (PubMed ID: 26911353)

  • 1. 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]  

  • 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. Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophy.
    Wang Y; Yang Y; Liu J; Chen XC; Liu X; Wang CZ; He XY
    Mol Genet Genomics; 2014 Oct; 289(5):1013-21. PubMed ID: 24770780
    [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 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]  

  • 6. [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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform.
    Lim BC; Lee S; Shin JY; Kim JI; Hwang H; Kim KJ; Hwang YS; Seo JS; Chae JH
    J Med Genet; 2011 Nov; 48(11):731-6. PubMed ID: 21969337
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
    Murugan S; Chandramohan A; Lakshmi BR
    Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Improved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method.
    Sansović I; Barišić I; Dumić K
    Biochem Genet; 2013 Apr; 51(3-4):189-201. PubMed ID: 23224783
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A splicing mutation in the DMD gene detected by next-generation sequencing and confirmed by mRNA and protein analysis.
    Roucher Boulez F; Menassa R; Streichenberger N; Manel V; Mallet-Motak D; Morel Y; Michel-Calemard L
    Clin Chim Acta; 2015 Aug; 448():146-9. PubMed ID: 26148721
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Mutation Spectrum of Dystrophinopathies in India: Implications for Therapy.
    Kohli S; Saxena R; Thomas E; Singh K; Bijarnia Mahay S; Puri RD; Verma IC
    Indian J Pediatr; 2020 Jul; 87(7):495-504. PubMed ID: 32358784
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.
    Zhong J; Xu T; Chen G; Liao H; Zhang J; Lan D
    Muscle Nerve; 2017 Jul; 56(1):117-121. PubMed ID: 27750387
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of dystrophin gene in Iranian Duchenne and Becker muscular dystrophies patients and identification of a novel mutation.
    Zamani GR; Karami F; Mehdizadeh M; Movafagh A; Nilipour Y; Zamani M
    Neurol Sci; 2015 Nov; 36(11):2011-7. PubMed ID: 26081009
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients.
    Chaturvedi LS; Mukherjee M; Srivastava S; Mittal RD; Mittal B
    Exp Mol Med; 2001 Dec; 33(4):251-6. PubMed ID: 11795488
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene.
    Niba ET; Tran VK; Tuan-Pham le A; Vu DC; Nguyen NK; Ta VT; Tran TH; Lee T; Takeshima Y; Matsuo M
    Clin Chim Acta; 2014 Sep; 436():155-9. PubMed ID: 24892813
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiplex Ligation-Dependent Probe Amplification in X-linked Recessive Muscular Dystrophy in Korean Subjects.
    Suh MR; Lee KA; Kim EY; Jung J; Choi WA; Kang SW
    Yonsei Med J; 2017 May; 58(3):613-618. PubMed ID: 28332368
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 30.