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Journal Abstract Search

110 related items for PubMed ID: 20029221

  • 1. Potential errors with rapid analysis techniques: partial duplication 21q resulting from a paternal paracentric insertion uncovered in chorionic villus sampling by fluorescence in situ hybridization.
    Ehrhardt N, Kujat A, Faber R, Horn LC, Froster UG.
    Fetal Diagn Ther; 2009; 26(4):219-22. PubMed ID: 20029221
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  • 2. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
    Tardy EP, Tóth A, Kosztolányi G.
    Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
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  • 3. The clinical application of interphase FISH in prenatal diagnosis.
    Pergament E, Chen PX, Thangavelu M, Fiddler M.
    Prenat Diagn; 2000 Mar; 20(3):215-20. PubMed ID: 10719324
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  • 4. [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
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  • 5. [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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  • 9. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K, Tanemura M, Oya N, Suzumori N, Kim KC, Ohashi H, Fukushima Y.
    Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
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  • 11. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
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  • 12. 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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  • 13. [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 Feb; 200(5):186-90. PubMed ID: 9035828
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  • 15. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
    Hsieh LJ, Hsieh TC, Yeh GP, Lin MI, Chen M, Wang BB.
    Fetal Diagn Ther; 2004 Feb; 19(4):356-60. PubMed ID: 15192296
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  • 16. [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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  • 18. Investigation of bone marrow involvement in malignant lymphoma using fluorescence in situ hybridization: possible utility in the detection of micrometastasis.
    Huh HJ, Min HC, Cho HI, Chae SL, Lee DS.
    Cancer Genet Cytogenet; 2008 Oct; 186(1):1-5. PubMed ID: 18786435
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  • 19. Interphase fluorescence in situ hybridization in a Turner syndrome variant with IsoXq. A case report.
    Chang SD, Lin SL, Chen FP, Chu KK.
    J Reprod Med; 1996 Mar; 41(3):175-8. PubMed ID: 8778416
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  • 20. 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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