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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

270 related items for PubMed ID: 12376264

  • 1. [Application of PCR technique in genetic diagnosis of Duchenne/Becker muscular dystrophy].
    Liu YM, Feng ZC, Fang ZW.
    Di Yi Jun Yi Da Xue Xue Bao; 2002 Aug; 22(8):731-3. PubMed ID: 12376264
    [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. [Carrier genetic diagnosis of intron and/or exon-deletion Duchenne muscular dystrophy by microsatellite analysis and quantitative polymerase chain reaction].
    Huang W, Zhang C, Xie YM, Chen SL, Zhang WX, Yao XL, Zeng Y, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):72-5. PubMed ID: 17285549
    [Abstract] [Full Text] [Related]

  • 4. 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; 23(1):57-66. PubMed ID: 14695533
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.
    Malcov M, Ben-Yosef D, Schwartz T, Mey-Raz N, Azem F, Lessing JB, Amit A, Yaron Y.
    Prenat Diagn; 2005 Dec; 25(13):1200-5. PubMed ID: 16353285
    [Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. [Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR].
    Wu YL, Wu LQ, Li YP, Liu DE, Zeng Q, Zhu HY, Pan Q, Liang DS, Hu H, Long ZG, Li J, Dai HP, Xia K, Xia JH.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr 07; 32(2):246-51. PubMed ID: 17478931
    [Abstract] [Full Text] [Related]

  • 9. [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 07; 20(4):350-2. PubMed ID: 12903051
    [Abstract] [Full Text] [Related]

  • 10. 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 07; 19(2):108-12. PubMed ID: 19084397
    [Abstract] [Full Text] [Related]

  • 11. 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 07; 51(2):223-6. PubMed ID: 14571009
    [Abstract] [Full Text] [Related]

  • 12. Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.
    Zhu HY, Wu LQ, Liang DS, Pan Q, Xia JH.
    Yi Chuan Xue Bao; 2006 Mar 07; 33(3):206-12. PubMed ID: 16553208
    [Abstract] [Full Text] [Related]

  • 13. Valley sign in Becker muscular dystrophy and outliers of Duchenne and Becker muscular dystrophy.
    Pradhan S.
    Neurol India; 2004 Jun 07; 52(2):203-5. PubMed ID: 15269471
    [Abstract] [Full Text] [Related]

  • 14. 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 07; 18(8):667-70. PubMed ID: 18653336
    [Abstract] [Full Text] [Related]

  • 15. [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 07; 31(3):338-43. PubMed ID: 24928015
    [Abstract] [Full Text] [Related]

  • 16. [Molecular genetic characteristics of Duchenne-Becker muscular dystrophy in the Republic of Moldova].
    Sacare VK.
    Genetika; 2008 Oct 07; 44(10):1404-9. PubMed ID: 19062538
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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 15; 39(4):367-72. PubMed ID: 16413013
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 13(11):1231-4. PubMed ID: 16030524
    [Abstract] [Full Text] [Related]

  • 20. [Evaluation of multiplex PCR assay using dual priming oligonucleotide system for detection mutation in the Duchenne muscular dystrophy gene].
    Park Y, Kim J, Choi JR, Song J, Chung JS, Lee KA.
    Korean J Lab Med; 2008 Oct 15; 28(5):386-91. PubMed ID: 18971620
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.