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Journal Abstract Search

131 related items for PubMed ID: 8713667

  • 1. [Fluorescence in situ hybridization in prenatal diagnosis. First experiences].
    Tardy E, Tóth A, Hajdu K, Gombos S, László J.
    Orv Hetil; 1996 Mar 10; 137(10):523-6. PubMed ID: 8713667
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  • 2. [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 10; 17(2):120-4. PubMed ID: 7656391
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  • 3. [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 10; 32(11):646-8. PubMed ID: 9639761
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  • 4. Prenatal diagnosis with repetitive in situ hybridization probes.
    Lebo RV, Flandermeyer RR, Diukman R, Lynch ED, Lepercq JA, Golbus MS.
    Am J Med Genet; 1992 Jul 15; 43(5):848-54. PubMed ID: 1642274
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  • 5. [Application of inter-fluorescence in situ hybridization of chromosome 13/21 alpha satellite probe in amniotic cells for prenatal diagnosis trisomy 21 syndrome].
    Li W, Wu Y, Ye Z.
    Zhonghua Fu Chan Ke Za Zhi; 2001 Feb 15; 36(2):76-8. PubMed ID: 11783350
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 17(9):871-3. PubMed ID: 9316133
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  • 7. [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 15; 21(6):608-10. PubMed ID: 15583993
    [Abstract] [Full Text] [Related]

  • 8. [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 15; 22(3):317-9. PubMed ID: 15952125
    [Abstract] [Full Text] [Related]

  • 9. Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.
    Sullivan BA, Leana-Cox J, Schwartz S.
    Am J Med Genet; 1993 Aug 15; 47(2):223-30. PubMed ID: 8213910
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  • 10. [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 Aug 15; 200(5):186-90. PubMed ID: 9035828
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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 15; 23(2):146-51. PubMed ID: 12575023
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  • 13. Re: Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common aneuploidies by FISH.
    Blancato JK.
    Prenat Diagn; 1996 Aug 15; 16(8):769-70. PubMed ID: 8878290
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  • 20. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
    Darnaude MT, Diaz de Bustamante A, Cabello P, Vallcorba I.
    Ann Genet; 1996 Aug 15; 39(2):61-3. PubMed ID: 8766134
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