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PUBMED FOR HANDHELDS

Journal Abstract Search


516 related items for PubMed ID: 24040987

  • 1.
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  • 2. Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.
    Langlois S, Duncan A, SOGC GENETICS COMMITTEE, CCMG PRENATAL DIAGNOSIS COMMITTEE.
    J Obstet Gynaecol Can; 2011 Sep; 33(9):955-960. PubMed ID: 21923994
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  • 4. Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.
    Onay H, Ugurlu T, Aykut A, Pehlivan S, Inal M, Tinar S, Ozkinay C, Ozkinay F.
    Gynecol Obstet Invest; 2008 Sep; 66(2):104-10. PubMed ID: 18446039
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  • 6. Diagnostic accuracy of the BACs-on-Beads™ assay versus karyotyping for prenatal detection of chromosomal abnormalities: a retrospective consecutive case series.
    Choy KW, Kwok YK, Cheng YK, Wong KM, Wong HK, Leung KO, Suen KW, Adler K, Wang CC, Lau TK, Schermer MJ, Lao TT, Leung TY.
    BJOG; 2014 Sep; 121(10):1245-52. PubMed ID: 24893808
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  • 7. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP, Wu JP, Li XT, Lei CX, Xu JZ, Yin M.
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
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  • 8. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
    Donaghue C, Mann K, Docherty Z, Ogilvie CM.
    Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691
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  • 11. [Application of quantitative fluorescence PCR for the prenatal diagnosis of common fetal chromosomal aneuploidies].
    Liu X, Zhang Y, Cui W, He R, Zhao Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):635-40. PubMed ID: 26418981
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  • 13. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
    Xiao HM, Tan YQ, Li LY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
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  • 16. Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.
    Pan M, Han J, Zhen L, Yang X, Li R, Liao C, Li DZ.
    Eur J Obstet Gynecol Reprod Biol; 2016 Feb; 197():164-7. PubMed ID: 26771907
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  • 17. Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).
    Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP.
    Prenat Diagn; 2002 Jan; 22(1):29-33. PubMed ID: 11810646
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  • 18. Detection of sex chromosome aneuploidies using quantitative fluorescent PCR in the Hungarian population.
    Nagy B, Nagy RG, Lazar L, Schonleber J, Papp C, Rigo J.
    Clin Chim Acta; 2015 May 20; 445():2-6. PubMed ID: 25791892
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  • 19. Rapid prenatal diagnosis of aneuploidy by quantitative fluorescent PCR on fetal samples from mothers at high risk for chromosome disorders.
    Pertl B, Pieber D, Lercher-Hartlieb A, Orescovic I, Haeusler M, Winter R, Kroisel P, Adinolfi M.
    Mol Hum Reprod; 1999 Dec 20; 5(12):1176-9. PubMed ID: 10587374
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  • 20. Prenatal diagnosis of common aneuploidies using multiplex quantitative fluorescent polymerase chain reaction.
    El Mouatassim S, Becker M, Kuzio S, Ronsin C, Gil S, Nouchy M, Druard L, Forestier F.
    Fetal Diagn Ther; 2004 Dec 20; 19(6):496-503. PubMed ID: 15539874
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