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Journal Abstract Search


437 related items for PubMed ID: 23224783

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.
    Dastur RS, Kachwala MY, Khadilkar SV, Hegde MR, Gaitonde PS.
    Neurol India; 2011 Apr; 59(6):803-9. PubMed ID: 22234189
    [Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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 Sep; 48(6):416-22. PubMed ID: 25482253
    [Abstract] [Full Text] [Related]

  • 6. Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).
    Lai KK, Lo IF, Tong TM, Cheng LY, Lam ST.
    Clin Biochem; 2006 Apr; 39(4):367-72. PubMed ID: 16413013
    [Abstract] [Full Text] [Related]

  • 7. A comparative study of mPCR, MLPA, and muscle biopsy results in a cohort of children with Duchenne muscular dystrophy: a first study.
    Manjunath M, Kiran P, Preethish-Kumar V, Nalini A, Singh RJ, Gayathri N.
    Neurol India; 2015 Apr; 63(1):58-62. PubMed ID: 25751470
    [Abstract] [Full Text] [Related]

  • 8. Deletion and duplication screening in the DMD gene using MLPA.
    Lalic T, Vossen RH, Coffa J, Schouten JP, Guc-Scekic M, Radivojevic D, Djurisic M, Breuning MH, White SJ, den Dunnen JT.
    Eur J Hum Genet; 2005 Nov; 13(11):1231-4. PubMed ID: 16030524
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. Genetic testing for Duchenne/Becker muscular dystrophy in Johannesburg, South Africa.
    Kerr R, Robinson C, Essop FB, Krause A.
    S Afr Med J; 2013 Oct 10; 103(12 Suppl 1):999-1004. PubMed ID: 24300647
    [Abstract] [Full Text] [Related]

  • 11. Dystrophin gene mutation analysis in Iranian males and females using multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification methods.
    Khordadpoor-Deilamani F, Akbari MT, Nafissi S, Zamani G.
    Genet Test Mol Biomarkers; 2011 Dec 10; 15(12):893-9. PubMed ID: 21815800
    [Abstract] [Full Text] [Related]

  • 12. [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]

  • 13. 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 10; 58(3):613-618. PubMed ID: 28332368
    [Abstract] [Full Text] [Related]

  • 14. [Clinical application of multiplex ligation-dependent probe amplification for the detection exonic copy number alterations in the Dystrophin gene].
    Long F, Sun W, Ji X, Li XH, Liu XQ, Jiang WT, Tao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec 10; 28(6):699-704. PubMed ID: 22161109
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 60(2):112-7. PubMed ID: 24213305
    [Abstract] [Full Text] [Related]

  • 16. [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]

  • 17. 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 10; 18(8):667-70. PubMed ID: 18653336
    [Abstract] [Full Text] [Related]

  • 18. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
    Pikó H, Vancsó V, Nagy B, Bán Z, Herczegfalvi A, Karcagi V.
    Neuromuscul Disord; 2009 Feb 10; 19(2):108-12. PubMed ID: 19084397
    [Abstract] [Full Text] [Related]

  • 19. [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 26; 96(16):1261-9. PubMed ID: 27122458
    [Abstract] [Full Text] [Related]

  • 20. Multiplex ligation-dependent probe amplification identification of deletions and duplications of the Duchenne muscular dystrophy gene in Taiwanese subjects.
    Hwa HL, Chang YY, Chen CH, Kao YS, Jong YJ, Chao MC, Ko TM.
    J Formos Med Assoc; 2007 May 26; 106(5):339-46. PubMed ID: 17561468
    [Abstract] [Full Text] [Related]


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