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701 related items for PubMed ID: 14571009

  • 1. 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]

  • 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
    [Abstract] [Full Text] [Related]

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

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

  • 5. 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]

  • 6. 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]

  • 7. Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophy.
    Pandey GS, Kesari A, Mukherjee M, Mittal RD, Mittal B.
    Neurol India; 2003 Sep; 51(3):367-9. PubMed ID: 14652441
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 18(8):667-70. PubMed ID: 18653336
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  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. [Deletions in the dystrophin gene and its phenotype expression].
    Lalić T, Guć-Sćekić M, Djurisić M, Radivojević D, Zamurović D, Todorović S.
    Srp Arh Celok Lek; 2001 Sep 15; 129 Suppl 1():3-5. PubMed ID: 15637982
    [Abstract] [Full Text] [Related]

  • 15. [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 15; 20(4):350-2. PubMed ID: 12903051
    [Abstract] [Full Text] [Related]

  • 16. Proximal dystrophin gene deletions and protein alterations in becker muscular dystrophy.
    Novaković I, Bojić D, Todorović S, Apostolski S, Luković L, Stefanović D, Milasin J.
    Ann N Y Acad Sci; 2005 Jun 15; 1048():406-10. PubMed ID: 16154963
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 42(12):1291-9. PubMed ID: 19439162
    [Abstract] [Full Text] [Related]

  • 18. DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
    Hofstra RM, Mulder IM, Vossen R, de Koning-Gans PA, Kraak M, Ginjaar IB, van der Hout AH, Bakker E, Buys CH, van Ommen GJ, van Essen AJ, den Dunnen JT.
    Hum Mutat; 2004 Jan 15; 23(1):57-66. PubMed ID: 14695533
    [Abstract] [Full Text] [Related]

  • 19. [From gene to disease; the dystrophin gene involved in Duchenne and Becker muscular dystrophy].
    den Dunnen JT, de Visser M, Bakker E.
    Ned Tijdschr Geneeskd; 2002 Feb 23; 146(8):364-7. PubMed ID: 11887623
    [Abstract] [Full Text] [Related]

  • 20. Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion.
    Lee KA, Han SH, Choi JR, Chung JS, Choi YC.
    Pediatr Neurol; 2008 Aug 23; 39(2):129-32. PubMed ID: 18639760
    [Abstract] [Full Text] [Related]

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