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Journal Abstract Search

926 related items for PubMed ID: 15583993

  • 1. [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]

  • 2. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
    Wang H, Li H, Wang H, Wang H, Xia Y, Wen J, Long Z, Dai H, Liang D, Xia J, Wu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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
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  • 8. [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 Apr; 204(1):1-7. PubMed ID: 10721179
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  • 9. Rapid prenatal diagnosis of Down syndrome using quantitative fluorescence in situ hybridization on interphase nuclei.
    Truong K, Gibaud A, Dupont JM, Guilly MN, Soussaline F, Dutrillaux B, Malfoy B.
    Prenat Diagn; 2003 Feb; 23(2):146-51. PubMed ID: 12575023
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  • 10. Fluorescence in situ hybridization in uncultured amniocytes for detection of aneuploidy in 4210 prenatal cases.
    Jia CW, Wang SY, Ma YM, Lan YL, Si YM, Yu L, Zhou LY.
    Chin Med J (Engl); 2011 Apr; 124(8):1164-8. PubMed ID: 21542989
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  • 11. Simultaneous identification of chromosomes 18, X and Y in uncultured amniocytes by using multi-primed in situ labelling technique.
    Gadji M, Krabchi K, Drouin R.
    Clin Genet; 2005 Jul; 68(1):15-22. PubMed ID: 15952981
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  • 12. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
    Graf MD, Gill P, Krew M, Schwartz S.
    Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization on uncultured amniotic cells: experience with 630 samples.
    Mercier S, Bresson JL.
    Ann Genet; 1995 Aug; 38(3):151-7. PubMed ID: 8540686
    [Abstract] [Full Text] [Related]

  • 14. [Rapid detection of numerical aberrations of chromosomes in the first trimester of pregnancy by using fluorescence in situ hybridization (FISH)].
    Xiang Y, Bryndorf T, Philip J, Sun N.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Apr; 17(2):120-4. PubMed ID: 7656391
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  • 15. Routine prenatal diagnosis of aneuploidy by FISH studies in high-risk pregnancies.
    Feldman B, Ebrahim SA, Hazan SL, Gyi K, Johnson MP, Johnson A, Evans MI.
    Am J Med Genet; 2000 Jan 31; 90(3):233-8. PubMed ID: 10678661
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  • 16. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
    Ogilvie CM, Donaghue C, Fox SP, Docherty Z, Mann K.
    J Histochem Cytochem; 2005 Mar 31; 53(3):285-8. PubMed ID: 15750003
    [Abstract] [Full Text] [Related]

  • 17. [Application of fluorescence in situ hybridization to prenatal diagnosis of Down syndrome].
    Wang M, Li QF, Qiao FY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun 31; 22(3):317-9. PubMed ID: 15952125
    [Abstract] [Full Text] [Related]

  • 18. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A, Röddiger S, Born HJ, Baier P, Halberstadt E.
    Z Geburtshilfe Neonatol; 1996 Jun 31; 200(5):186-90. PubMed ID: 9035828
    [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 31; 46(9):644-8. PubMed ID: 22176986
    [Abstract] [Full Text] [Related]

  • 20. Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
    Bryndorf T, Lundsteen C, Lamb A, Christensen B, Philip J.
    Acta Obstet Gynecol Scand; 2000 Jan 31; 79(1):8-14. PubMed ID: 10646809
    [Abstract] [Full Text] [Related]

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