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139 related items for PubMed ID: 11920892

  • 1. Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes.
    Pettenati MJ, Von Kap-Herr C, Jackle B, Bobby P, Mowrey P, Schwartz S, Rao PN, Rosnes J.
    Prenat Diagn; 2002 Mar; 22(3):193-7. PubMed ID: 11920892
    [Abstract] [Full Text] [Related]

  • 2. Rapid prenatal diagnosis in translocation carriers by interphase FISH with chromosome-specific subtelomere probes.
    Cotter PD, Musci TJ, Norton ME.
    Am J Med Genet A; 2003 Sep 15; 122A(1):1-5. PubMed ID: 12949964
    [Abstract] [Full Text] [Related]

  • 3. Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
    Cotter PD, Musci TJ.
    Prenat Diagn; 2001 Mar 15; 21(3):171-5. PubMed ID: 11260602
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 22(1):29-33. PubMed ID: 11810646
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 20(4):275-80. PubMed ID: 10740198
    [Abstract] [Full Text] [Related]

  • 6. Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization.
    Cacheux V, Tachdjian G, Druart L, Oury JF, Sérero S, Blot P, Nessmann C.
    Prenat Diagn; 1994 Feb 15; 14(2):79-86. PubMed ID: 8183853
    [Abstract] [Full Text] [Related]

  • 7. 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 15; 79(1):8-14. PubMed ID: 10646809
    [Abstract] [Full Text] [Related]

  • 8. Prenatal detection of aneuploidy by directly labeled multicolored probes and interphase fluorescence in situ hybridization.
    Jalal SM, Law ME, Carlson RO, Dewald GW.
    Mayo Clin Proc; 1998 Feb 15; 73(2):132-7. PubMed ID: 9472995
    [Abstract] [Full Text] [Related]

  • 9. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP, Chern SR, Wu PC, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2009 Dec 15; 48(4):389-99. PubMed ID: 20045761
    [Abstract] [Full Text] [Related]

  • 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 Dec 15; 200(5):186-90. PubMed ID: 9035828
    [Abstract] [Full Text] [Related]

  • 11. Rapid detection of aneuploidy in uncultured chorionic villus cells using fluorescence in situ hybridization.
    Rao PN, Hayworth R, Cox K, Grass F, Pettenati MJ.
    Prenat Diagn; 1993 Apr 15; 13(4):233-8. PubMed ID: 8506226
    [Abstract] [Full Text] [Related]

  • 12. Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes.
    Kuo WL, Tenjin H, Segraves R, Pinkel D, Golbus MS, Gray J.
    Am J Hum Genet; 1991 Jul 15; 49(1):112-9. PubMed ID: 2063863
    [Abstract] [Full Text] [Related]

  • 13. Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.
    Pettenati MJ, Jackle B, Bobby P, Stewart W, Von Kap-Herr C, Mowrey P, Rao PN, May KM.
    Am J Med Genet; 2002 Jul 22; 111(1):48-53. PubMed ID: 12124733
    [Abstract] [Full Text] [Related]

  • 14. Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate.
    Silverstein S, Lerer I, Sagi M, Frumkin A, Ben-Neriah Z, Abeliovich D.
    Prenat Diagn; 2002 Aug 22; 22(8):649-51. PubMed ID: 12210570
    [Abstract] [Full Text] [Related]

  • 15. Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements.
    Souter VL, Glass IA, Chapman DB, Raff ML, Parisi MA, Opheim KE, Disteche CM.
    Ultrasound Obstet Gynecol; 2003 Jun 22; 21(6):609-15. PubMed ID: 12808681
    [Abstract] [Full Text] [Related]

  • 16. Detection of translocations involving the Y-chromosome in prospective prenatal screening of common chromosomal aneuploidies by FISH.
    Verlinsky Y, Ginsberg N, Chmura M, White M, Strom C, Kuliev A.
    Prenat Diagn; 1998 Apr 22; 18(4):390-2. PubMed ID: 9602488
    [Abstract] [Full Text] [Related]

  • 17. Detection of newborn aneuploidy by interphase fluorescence in situ hybridization.
    Jalal SM, Law ME.
    Mayo Clin Proc; 1997 Aug 22; 72(8):705-10. PubMed ID: 9276596
    [Abstract] [Full Text] [Related]

  • 18. Prenatal detection of aneuploidies using fluorescence in situ hybridization: a preliminary experience in an Indian set up.
    Jobanputra V, Roy KK, Kucheria K.
    J Biosci; 2002 Mar 22; 27(2):155-63. PubMed ID: 11937686
    [Abstract] [Full Text] [Related]

  • 19. The clinical application of interphase FISH in prenatal diagnosis.
    Pergament E, Chen PX, Thangavelu M, Fiddler M.
    Prenat Diagn; 2000 Mar 22; 20(3):215-20. PubMed ID: 10719324
    [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; 2000 Mar 22; 366(9480):123-8. PubMed ID: 16005334
    [Abstract] [Full Text] [Related]

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