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Journal Abstract Search

509 related items for PubMed ID: 11810646

  • 1. 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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  • 2. [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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  • 5. [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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  • 6. 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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  • 7. [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
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  • 9. An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis.
    Thein AT, Abdel-Fattah SA, Kyle PM, Soothill PW.
    Prenat Diagn; 2000 Apr; 20(4):275-80. PubMed ID: 10740198
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  • 13. Rapid one-day fluorescence in situ hybridisation in prenatal diagnosis using uncultured amniocytes and chorionic villi.
    Cai LS, Lim AS, Tan A.
    Ann Acad Med Singap; 1999 Jul; 28(4):502-7. PubMed ID: 10561761
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  • 14. [Interphase FISH test as a rapid test for trisomies in amniotic fluid--results of a prospective study].
    Bink K, Pauer HU, Bartels I.
    Z Geburtshilfe Neonatol; 2000 Jul; 204(1):8-13. PubMed ID: 10721180
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  • 16. Analysis of amniotic fluid specimens for common chromosome disorders using interphase fluorescence in situ hybridization.
    Moatter T, Khilji Z, Murad F, Munim S.
    J Pak Med Assoc; 2007 Apr; 57(4):189-92. PubMed ID: 17489527
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  • 18. [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
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  • 20. Prenatal diagnosis with use of fetal cells isolated from maternal blood: five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21.
    Bischoff FZ, Lewis DE, Nguyen DD, Murrell S, Schober W, Scott J, Simpson JL, Elias S.
    Am J Obstet Gynecol; 1998 Jul; 179(1):203-9. PubMed ID: 9704788
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