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

235 related items for PubMed ID: 16553208

  • 1. 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; 33(3):206-12. PubMed ID: 16553208
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of Duchenne/Becker muscular dystrophy by short tandem repeat segregation analysis in Argentine families.
    Giliberto F, Ferreiro V, Massot F, Ferrer M, Francipane L, Szijan I.
    Muscle Nerve; 2011 Apr; 43(4):510-7. PubMed ID: 21305566
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [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; 30(1):45-8. PubMed ID: 23450478
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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]

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

  • 11. [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]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Gene deletion and carrier detection in the family of Becker muscular dystrophy by short tandem repeat sequence polymorphism.
    Cai S, Shen D, Wang J.
    Chin Med J (Engl); 1999 Mar; 112(3):242-5. PubMed ID: 11593558
    [Abstract] [Full Text] [Related]

  • 16. [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
    [Abstract] [Full Text] [Related]

  • 17. Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India.
    Purushottam M, Murthy AR, Shubha GN, Gayathri N, Nalini A.
    J Neurol Sci; 2008 May 15; 268(1-2):179-82. PubMed ID: 18031759
    [Abstract] [Full Text] [Related]

  • 18. Comparison of serum creatine kinase estimation with short tandem repeats based linkage analysis in carriers and affected children of Duchenne muscular dystrophy.
    Hashim R, Shaheen S, Ahmad S, Sattar A, Khan FA.
    J Ayub Med Coll Abbottabad; 2011 May 15; 23(1):125-8. PubMed ID: 22830166
    [Abstract] [Full Text] [Related]

  • 19. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene.
    Deburgrave N, Daoud F, Llense S, Barbot JC, Récan D, Peccate C, Burghes AH, Béroud C, Garcia L, Kaplan JC, Chelly J, Leturcq F.
    Hum Mutat; 2007 Feb 15; 28(2):183-95. PubMed ID: 17041906
    [Abstract] [Full Text] [Related]

  • 20. Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification.
    Ren Z, Zeng HT, Xu YW, Zhuang GL, Deng J, Zhang C, Zhou CQ.
    Fertil Steril; 2009 Feb 15; 91(2):359-64. PubMed ID: 18359022
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.