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728 related items for PubMed ID: 16005334

  • 1. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment.
    Caine A, Maltby AE, Parkin CA, Waters JJ, Crolla JA, UK Association of Clinical Cytogeneticists (ACC).
    Lancet; ; 366(9480):123-8. PubMed ID: 16005334
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testing.
    Ogilvie CM, Lashwood A, Chitty L, Waters JJ, Scriven PN, Flinter F.
    BJOG; 2005 Oct; 112(10):1369-75. PubMed ID: 16167939
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second-trimester amniocenteses.
    Leung WC, Waters JJ, Chitty L.
    Prenat Diagn; 2004 Oct; 24(10):790-5. PubMed ID: 15503279
    [Abstract] [Full Text] [Related]

  • 5. [Rapid prenatal diagnosis of Down's syndrome in the first trimester of pregnancy by fluorescence in situ hybridization].
    Xiang Y, Sun N, Wang F.
    Zhonghua Fu Chan Ke Za Zhi; 1997 Nov; 32(11):646-8. PubMed ID: 9639761
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Prenatal screening using maternal serum alpha-fetoprotein, human chorionic gonadotropin, and unconjugated estriol: two-year experience in a health maintenance organization.
    McDuffie RS, Haverkamp AD, Stark CF, Haverkamp C, Barth CK.
    J Matern Fetal Med; 1996 Jan; 5(2):70-3. PubMed ID: 8796771
    [Abstract] [Full Text] [Related]

  • 8. [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
    [Abstract] [Full Text] [Related]

  • 9. Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reaction.
    Ochshorn Y, Bar-Shira A, Jonish A, Yaron Y.
    Fetal Diagn Ther; 2006 Dec; 21(4):326-31. PubMed ID: 16757905
    [Abstract] [Full Text] [Related]

  • 10. Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases.
    Weremowicz S, Sandstrom DJ, Morton CC, Niedzwiecki CA, Sandstrom MM, Bieber FR.
    Prenat Diagn; 2001 Apr; 21(4):262-9. PubMed ID: 11288114
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. [Future of prenatal cytogenetic studies: rapid aneuploidy testing or full karyotype].
    Bocian E.
    Ginekol Pol; 2007 Nov; 78(11):881-7. PubMed ID: 18306922
    [Abstract] [Full Text] [Related]

  • 13. [Application of fluorescence in situ hybridization to prenatal diagnosis of aneuploidy in 110 uncultured amniotic fluid samples].
    Liu H, Liao C, Huang YN, Pan M, Yi CX, Yuan SM, Hu SY, Zhong HZ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):453-6. PubMed ID: 20677157
    [Abstract] [Full Text] [Related]

  • 14. [Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].
    Wang SJ, Gao ZY, Lu YP, Li YL, You YQ, Zhang LW, Wang LX, Xu H.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Nov; 47(11):808-12. PubMed ID: 23302119
    [Abstract] [Full Text] [Related]

  • 15. Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
    Petersen AK, Cheung SW, Smith JL, Bi W, Ward PA, Peacock S, Braxton A, Van Den Veyver IB, Breman AM.
    Am J Obstet Gynecol; 2017 Dec; 217(6):691.e1-691.e6. PubMed ID: 29032050
    [Abstract] [Full Text] [Related]

  • 16. [Clinical application of noninvasive prenatal diagnosis using cell free fetal DNA in maternal plasma].
    Hou QF, Wu D, Chu Y, Kang B, Liao SX, Yang YL, Zhang CY, Zhang JX, Wu G.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Nov; 47(11):813-7. PubMed ID: 23302120
    [Abstract] [Full Text] [Related]

  • 17. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R, Pfeiffer RA, Kollert A, Beinder E.
    Z Geburtshilfe Neonatol; 2000 Nov; 204(1):1-7. PubMed ID: 10721179
    [Abstract] [Full Text] [Related]

  • 18. The replacement of cytogenetic analysis by direct chorionic villi sampling preparation with quantitative fluorescence PCR.
    Christopoulou S, Christopoulou G, Hatzaki A, Hatzipouliou A, Donoghue J, Karkaletsi M, Kaminopetros P, Sifakis S, Velissariou V.
    Gynecol Obstet Invest; 2009 Nov; 68(4):255-61. PubMed ID: 19776613
    [Abstract] [Full Text] [Related]

  • 19. [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
    [Abstract] [Full Text] [Related]

  • 20. [Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR].
    Švecová I, Burjanivová T, Kršiaková J, Lasabová Z, Biringer K, Kapustová I, Móricová P, Danko J.
    Ceska Gynekol; 2013 Aug; 78(4):373-8. PubMed ID: 24040987
    [Abstract] [Full Text] [Related]

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