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Journal Abstract Search

434 related items for PubMed ID: 10854113

  • 1. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
    Ligon AH, Kashork CD, Richards CS, Shaffer LG.
    Eur J Hum Genet; 2000 Apr; 8(4):293-8. PubMed ID: 10854113
    [Abstract] [Full Text] [Related]

  • 2. [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
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  • 4. 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; 19(2):108-12. PubMed ID: 19084397
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  • 5. [Detection of the gene-deleted female carriers of Duchenne/Becker muscular dystrophy using a fluorescent in situ hybridization based method].
    Qi QW, Sun NH, Hao N.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):350-2. PubMed ID: 12903051
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  • 7. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
    Kumari D, Mital A, Gupta M, Goyle S.
    Neurol India; 2003 Jun; 51(2):223-6. PubMed ID: 14571009
    [Abstract] [Full Text] [Related]

  • 8. 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
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  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. [Carrier detection of Duchenne/Becker muscular dystrophy by analysis of STRs loci linked to the gene of dystrophin in Venezuelan families].
    Delgado-Luengo WN, Borjas-Fuentes L, Zabala-Fernández W, Fernández-Salgado E, Solís-Añez E, Chávez C, Martínez-Basalo C, González-Ferrer S, Rojas-Atencio A, Morales-Machin A, Peña J, Pineda-Bernal L, González R, Miranda LE, Delgado-Luengo J, Hernández ML, Chacín JA, Quintero M.
    Invest Clin; 2002 Dec; 43(4):239-54. PubMed ID: 12520997
    [Abstract] [Full Text] [Related]

  • 11. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
    Al-Jumah M, Majumdar R, Al-Rajeh S, Chaves-Carballo E, Salih MM, Awada A, Al-Shahwan S, Al-Uthaim S.
    Saudi Med J; 2002 Dec; 23(12):1478-82. PubMed ID: 12518196
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  • 13. Validation and comparison of two quantitative real-time PCR assays for direct detection of DMD/BMD carriers.
    Hayat Nosaeid M, Mahdian R, Jamali S, Maryami F, Babashah S, Maryami F, Karimipoor M, Zeinali S.
    Clin Biochem; 2009 Aug; 42(12):1291-9. PubMed ID: 19439162
    [Abstract] [Full Text] [Related]

  • 14. Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.
    Hallwirth Pillay KD, Bill PL, Madurai S, Mubaiwa L, Rapiti P.
    J Neurol Sci; 2007 Jan 15; 252(1):1-3. PubMed ID: 17141273
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 132():303-11. PubMed ID: 20847377
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  • 16. [Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].
    Zhu HY, Li J, Yang Y, Wu X, Zhu XY, Zhu RF, Zhang Y, Duan HL, Hu YL.
    Zhonghua Yi Xue Za Zhi; 2009 Jul 07; 89(25):1753-6. PubMed ID: 19862979
    [Abstract] [Full Text] [Related]

  • 17. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
    Tuffery-Giraud S, Chambert S, Demaille J, Claustres M.
    Ann Biol Clin (Paris); 1999 Jul 07; 57(4):417-26. PubMed ID: 10432364
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  • 18. 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 Jul 07; 48(6):416-22. PubMed ID: 25482253
    [Abstract] [Full Text] [Related]

  • 19. [Detection of genomic duplications and deletions of the DMD gene in affected males and female carriers by using mutiplex ligation-dependent probe amplification].
    Shen BC, Zhang C, Sun XF, Zhang HM, Li SY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 07; 24(4):460-3. PubMed ID: 17680544
    [Abstract] [Full Text] [Related]

  • 20. 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 31; 33(4):251-6. PubMed ID: 11795488
    [Abstract] [Full Text] [Related]

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