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

198 related items for PubMed ID: 1513470

  • 1. Detection of Duchenne and Becker muscular dystrophy carriers by quantitative multiplex polymerase chain reaction analysis.
    Ioannou P, Christopoulos G, Panayides K, Kleanthous M, Middleton L.
    Neurology; 1992 Sep; 42(9):1783-90. PubMed ID: 1513470
    [Abstract] [Full Text] [Related]

  • 2. Molecular genetic detection of Xp21 muscular dystrophy carriers in Cyprus.
    Christodoulou K, Ioannou P, Middleton L.
    Biomed Pharmacother; 1994 Sep; 48(8-9):355-8. PubMed ID: 7858171
    [Abstract] [Full Text] [Related]

  • 3. Carrier detection and microsatellite analysis of Duchenne and Becker muscular dystrophy in Spanish families.
    Kruyer H, Miranda M, Volpini V, Estivill X.
    Prenat Diagn; 1994 Feb; 14(2):123-30. PubMed ID: 7910399
    [Abstract] [Full Text] [Related]

  • 4. Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.
    Schwartz LS, Tarleton J, Popovich B, Seltzer WK, Hoffman EP.
    Am J Hum Genet; 1992 Oct; 51(4):721-9. PubMed ID: 1415217
    [Abstract] [Full Text] [Related]

  • 5. The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis.
    Ferreiro V, Giliberto F, Francipane L, Szijan I.
    Mol Diagn; 2005 Oct; 9(2):67-80. PubMed ID: 16137182
    [Abstract] [Full Text] [Related]

  • 6. Detection of carriers of deletions in the dystrophin gene in Bulgarian DMD-BMD families.
    Bronzova J, Todorova A, Kalaydjieva L.
    Hum Genet; 1994 Feb; 93(2):170-4. PubMed ID: 8112741
    [Abstract] [Full Text] [Related]

  • 7. Identification of carriers of Duchenne/Becker muscular dystrophy by a novel method based on detection of junction fragments in the dystrophin gene.
    Yamagishi H, Kato S, Hiraishi Y, Ishihara T, Hata J, Matsuo N, Takano T.
    J Med Genet; 1996 Dec; 33(12):1027-31. PubMed ID: 9004137
    [Abstract] [Full Text] [Related]

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

  • 9. [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]

  • 10. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
    Darras BT, Blattner P, Harper JF, Spiro AJ, Alter S, Francke U.
    Am J Hum Genet; 1988 Nov; 43(5):620-9. PubMed ID: 2903663
    [Abstract] [Full Text] [Related]

  • 11. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
    Zhao W, Jiang N, Li S, Li JS, Miao Y, Liang SY, Yu DY.
    Zhonghua Fu Chan Ke Za Zhi; 2019 Apr 25; 54(4):226-231. PubMed ID: 31006187
    [Abstract] [Full Text] [Related]

  • 12. Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides.
    Prior TW, Papp AC, Snyder PJ, Highsmith WE, Friedman KJ, Perry TR, Silverman LM, Mendell JR.
    Clin Chem; 1990 Dec 25; 36(12):2113-7. PubMed ID: 2253356
    [Abstract] [Full Text] [Related]

  • 13. Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry.
    Allingham-Hawkins DJ, McGlynn-Steele LK, Brown CA, Sutherland J, Ray PN.
    Am J Med Genet; 1998 Jan 13; 75(2):171-5. PubMed ID: 9450879
    [Abstract] [Full Text] [Related]

  • 14. EVALUATION OF MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION AS A TOOL FOR DIAGNOSIS AND CARRIER DETECTION IN FAMILIES WITH A DYSTROPHINOPATHY.
    Salian S, Vahab SA, Shah H, Shukla A, Ramamurthy B, Shenoy R, Kamath N, Shenoy J, Satyamoorthy K, Girisha KM.
    Genet Couns; 2016 Jan 13; 27(4):449-460. PubMed ID: 30226963
    [Abstract] [Full Text] [Related]

  • 15. [Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].
    Grinchuk OV, Khidiiatova IM, Kiselev AV, Magzhanov RV, Khusnutdinova EK.
    Genetika; 1999 Apr 13; 35(4):551-5. PubMed ID: 10420280
    [Abstract] [Full Text] [Related]

  • 16. Carrier detection of Duchenne/Becker muscular dystrophy: computer-assisted direct quantitation of gene amplification products.
    Ishii K, Sakuraba H, Minamikawa-Tachino R, Shimmoto M, Suzuki Y.
    Brain Dev; 1992 Mar 13; 14(2):80-3. PubMed ID: 1621929
    [Abstract] [Full Text] [Related]

  • 17. Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA.
    Roberts RG, Bentley DR, Barby TF, Manners E, Bobrow M.
    Lancet; 1992 Mar 13; 336(8730):1523-6. PubMed ID: 1979364
    [Abstract] [Full Text] [Related]

  • 18. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.
    Claustres M, Tuffery S, Chevron MP, Jozelon MP, Martinez P, Echenne B, Demaille J.
    Hum Genet; 1991 Dec 13; 88(2):179-84. PubMed ID: 1684565
    [Abstract] [Full Text] [Related]

  • 19. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization.
    Rosenberg C, Navajas L, Vagenas DF, Bakker E, Vainzof M, Passos-Bueno MR, Takata RI, Van Ommen GJ, Zatz M, Den Dunnen JT.
    Neuromuscul Disord; 1998 Oct 13; 8(7):447-52. PubMed ID: 9829273
    [Abstract] [Full Text] [Related]

  • 20. High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling.
    Alcántara MA, Villarreal MT, Del Castillo V, Gutiérrez G, Saldaña Y, Maulen I, Lee R, Macías M, Orozco L.
    Clin Genet; 1999 May 13; 55(5):376-80. PubMed ID: 10422811
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.