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

176 related items for PubMed ID: 7823533

  • 21. Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin.
    Le Thiet Thanh, Nguyen Thi Man, Hori S, Sewry CA, Dubowitz V, Morris GE.
    Am J Med Genet; 1995 Aug 28; 58(2):177-86. PubMed ID: 8533812
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Multiplex PCR to detect the dystrophin gene deletion in Thai patients.
    Mutirangura A, Jongpiputvanich S, Norapucsunton T, Theamboonlers A, Srivuthana S, Promchainant C, Tumwasorn S, Sueblinvong T.
    J Med Assoc Thai; 1995 Sep 28; 78(9):460-5. PubMed ID: 7561572
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophy.
    Coral-Vázquez R, Arenas D, Cisneros B, Peñaloza L, Kofman S, Salamanca F, Montañez C.
    Arch Med Res; 1993 Sep 28; 24(1):1-6. PubMed ID: 8292871
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Comparative study on deletions of the dystrophin gene in three Asian populations.
    Lai PS, Takeshima Y, Adachi K, Van Tran K, Nguyen HT, Low PS, Matsuo M.
    J Hum Genet; 2002 Sep 28; 47(10):552-5. PubMed ID: 12376747
    [Abstract] [Full Text] [Related]

  • 28. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
    Sertić J, Barisić N, Sostarko M, Brzović Z, Stavljenić-Rukavina A.
    Coll Antropol; 1997 Jun 28; 21(1):151-6. PubMed ID: 9225508
    [Abstract] [Full Text] [Related]

  • 29. Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arrays.
    Graham IR, Hill VJ, Manoharan M, Inamati GB, Dickson G.
    J Gene Med; 2004 Oct 28; 6(10):1149-58. PubMed ID: 15386737
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Point mutations in Czech DMD/BMD patients and their phenotypic outcome.
    Sedlácková J, Vondrácek P, Hermanová M, Zámecník J, Hrubá Z, Haberlová J, Kraus J, Maríková T, Hedvicáková P, Vohánka S, Fajkusová L.
    Neuromuscul Disord; 2009 Nov 28; 19(11):749-53. PubMed ID: 19783145
    [Abstract] [Full Text] [Related]

  • 33. [Detection of extensive deletions and duplications in the dystrophin gene].
    Fajkusová L, Kuhrová V, Hájek J, Fajkus J.
    Cas Lek Cesk; 1997 Mar 12; 136(5):148-50. PubMed ID: 9221188
    [Abstract] [Full Text] [Related]

  • 34. [Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan].
    Odinokova ON, Puzyrev VP, Radzhabaliev ShF, Rakhmonov RA.
    Genetika; 1996 Oct 12; 32(10):1392-5. PubMed ID: 9091412
    [Abstract] [Full Text] [Related]

  • 35. 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 12; 39(4):367-72. PubMed ID: 16413013
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. 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 Apr 12; 48(6):416-22. PubMed ID: 25482253
    [Abstract] [Full Text] [Related]

  • 40. Identification of point mutations in Turkish DMD/BMD families using multiplex-single stranded conformation analysis (SSCA).
    Eraslan S, Kayserili H, Apak MY, Kirdar B.
    Eur J Hum Genet; 1999 Apr 12; 7(7):765-70. PubMed ID: 10573008
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.