These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

259 related items for PubMed ID: 7656391

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. [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]

  • 4. First-trimester prenatal diagnosis performed on pregnant women with fetal ultrasound abnormalities: the reliability of interphase fluorescence in situ hybridization (FISH) on mesenchymal core for the main aneuploidies.
    Toutain J, Epiney M, Begorre M, Dessuant H, Vandenbossche F, Horovitz J, Saura R.
    Eur J Obstet Gynecol Reprod Biol; 2010 Apr; 149(2):143-6. PubMed ID: 20045588
    [Abstract] [Full Text] [Related]

  • 5. [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 Apr; 200(5):186-90. PubMed ID: 9035828
    [Abstract] [Full Text] [Related]

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

  • 7. Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells.
    Bryndorf T, Christensen B, Xiang Y, Lind AM, Philip J.
    Prenat Diagn; 1993 Sep 10; 13(9):815-23. PubMed ID: 8278312
    [Abstract] [Full Text] [Related]

  • 8. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.
    Chin Med J (Engl); 2003 Sep 10; 116(9):1298-303. PubMed ID: 14527352
    [Abstract] [Full Text] [Related]

  • 9. Detection of chromosomal abnormalities using fluorescence in situ hybridization (FISH).
    Jobanputra V, Kriplani A, Choudhry VP, Kucheria K.
    Natl Med J India; 1998 Sep 10; 11(6):259-63. PubMed ID: 10083791
    [Abstract] [Full Text] [Related]

  • 10. 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 10; 79(1):8-14. PubMed ID: 10646809
    [Abstract] [Full Text] [Related]

  • 11. Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies.
    Morris A, Boyd E, Dhanjal S, Lowther GW, Aitken DA, Young J, Menzies AL, Imrie SJ, Connor JM.
    Prenat Diagn; 1999 Jun 10; 19(6):546-51. PubMed ID: 10416971
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. [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]

  • 15. The clinical application of interphase FISH in prenatal diagnosis.
    Pergament E, Chen PX, Thangavelu M, Fiddler M.
    Prenat Diagn; 2000 Mar 15; 20(3):215-20. PubMed ID: 10719324
    [Abstract] [Full Text] [Related]

  • 16. 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 Mar 15; 26(4):219-22. PubMed ID: 20029221
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 21(4):262-9. PubMed ID: 11288114
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. [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 15; 27(4):453-6. PubMed ID: 20677157
    [Abstract] [Full Text] [Related]

  • 20. 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; 2010 Aug 15; 366(9480):123-8. PubMed ID: 16005334
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.