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Journal Abstract Search

728 related items for PubMed ID: 16005334

  • 21. Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS.
    Allen SK, Luharia A, Gould CP, MacDonald F, Larkins S, Davison EV.
    Prenat Diagn; 2006 Dec; 26(12):1160-7. PubMed ID: 17063531
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  • 24. Rapid aneuploidy testing, traditional karyotyping, or both?
    Leung WC, Lao TT.
    Lancet; 2006 Dec; 366(9480):97-8. PubMed ID: 16005312
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  • 25. [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 Dec; 204(1):8-13. PubMed ID: 10721180
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  • 26. Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings.
    Meck JM, Kramer Dugan E, Matyakhina L, Aviram A, Trunca C, Pineda-Alvarez D, Aradhya S, Klein RT, Cherry AM.
    Am J Obstet Gynecol; 2015 Aug; 213(2):214.e1-5. PubMed ID: 25843063
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  • 27. [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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  • 28. Diagnostic performance of quantitative fluorescence PCR analysis in high-risk pregnancies after combined first-trimester screening.
    Lildballe DL, Vogel I, Petersen OB, Vestergaard EM.
    Dan Med J; 2014 Nov; 61(11):A4964. PubMed ID: 25370964
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  • 32. Prenatal detection of isochromosome 21 by QF-PCR. A comparison between FISH and traditional karyotyping.
    Gole L, Lian NB, Lian NP, Rauff M, Biswas A, Choolani M.
    Fetal Diagn Ther; 2008 Nov; 24(1):47-50. PubMed ID: 18504381
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  • 33. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
    Ogilvie CM, Donaghue C, Fox SP, Docherty Z, Mann K.
    J Histochem Cytochem; 2005 Mar; 53(3):285-8. PubMed ID: 15750003
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  • 34. 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; 26(4):219-22. PubMed ID: 20029221
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  • 36. Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.
    Brisset S, Aboura A, Audibert F, Costa JM, L'Herminé AC, Gautier V, Frydman R, Tachdjian G.
    Prenat Diagn; 2003 Jun; 23(6):461-9. PubMed ID: 12813759
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  • 38. [Rapid diagnosis of Down's and Edward's syndrome by multiplex real-time quantitative PCR].
    Sui JZ, Zhang HM, Sun XF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):449-52. PubMed ID: 20677156
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  • 39. 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; 79(1):8-14. PubMed ID: 10646809
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  • 40. Prenatal cytogenetic diagnosis in Spain: analysis and evaluation of the results obtained from amniotic fluid samples during the last decade.
    Mademont-Soler I, Morales C, Clusellas N, Soler A, Sánchez A, Group of Cytogenetics from Hospital Clínic de Barcelona.
    Eur J Obstet Gynecol Reprod Biol; 2011 Aug; 157(2):156-60. PubMed ID: 21492994
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