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181 related items for PubMed ID: 15130310

  • 1. [Short tandem repeat polymerase chain reaction used in prenatal diagnoses of the zygosity and common chromosomal trisomies in multiple pregnancies].
    Fang Q, An N, Wu XY, Liu QL, Feng SH.
    Zhonghua Yi Xue Za Zhi; 2004 Apr 17; 84(8):667-70. PubMed ID: 15130310
    [Abstract] [Full Text] [Related]

  • 2. Rapid prenatal diagnosis of aneuploidies and zygosity in multiple pregnancies by amniocentesis with single insertion of the needle and quantitative fluorescent PCR.
    Cirigliano V, Cañadas P, Plaja A, Ordoñez E, Mediano C, Sánchez A, Farrán I.
    Prenat Diagn; 2003 Aug 17; 23(8):629-33. PubMed ID: 12913868
    [Abstract] [Full Text] [Related]

  • 3. Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.
    Onay H, Ugurlu T, Aykut A, Pehlivan S, Inal M, Tinar S, Ozkinay C, Ozkinay F.
    Gynecol Obstet Invest; 2008 Aug 17; 66(2):104-10. PubMed ID: 18446039
    [Abstract] [Full Text] [Related]

  • 4. Prenatal detection of trisomy 13 from amniotic fluid by quantitative fluorescent polymerase chain reaction.
    Tóth T, Findlay I, Papp C, Tóth-Pál E, Marton T, Nagy B, Quirke P, Papp Z.
    Prenat Diagn; 1998 Jul 17; 18(7):669-74. PubMed ID: 9706647
    [Abstract] [Full Text] [Related]

  • 5. A prospective analysis of cell-free fetal DNA concentration in maternal plasma as an indicator for adverse pregnancy outcome.
    Bauer M, Hutterer G, Eder M, Majer S, Leshane E, Johnson KL, Peter I, Bianchi DW, Pertl B.
    Prenat Diagn; 2006 Sep 17; 26(9):831-6. PubMed ID: 16832830
    [Abstract] [Full Text] [Related]

  • 6. Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reaction.
    Ochshorn Y, Bar-Shira A, Jonish A, Yaron Y.
    Fetal Diagn Ther; 2006 Sep 17; 21(4):326-31. PubMed ID: 16757905
    [Abstract] [Full Text] [Related]

  • 7. Fetal pyelectasis: does fetal gender modify the risk of major trisomies?
    Bornstein E, Barnhard Y, Donnenfeld A, Ferber A, Divon MY.
    Obstet Gynecol; 2006 Apr 17; 107(4):877-9. PubMed ID: 16582126
    [Abstract] [Full Text] [Related]

  • 8. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
    Donaghue C, Mann K, Docherty Z, Ogilvie CM.
    Prenat Diagn; 2005 Jan 17; 25(1):65-72. PubMed ID: 15662691
    [Abstract] [Full Text] [Related]

  • 9. Multiplex fluorescent PCR for noninvasive prenatal detection of fetal-derived paternally inherited diseases using circulatory fetal DNA in maternal plasma.
    Tang DL, Li Y, Zhou X, Li X, Zheng F.
    Eur J Obstet Gynecol Reprod Biol; 2009 May 17; 144(1):35-9. PubMed ID: 19285775
    [Abstract] [Full Text] [Related]

  • 10. Determination of twin zygosity using a commercially available STR analysis of 15 unlinked loci and the gender-determining marker amelogenin--a preliminary report.
    Yang MJ, Tzeng CH, Tseng JY, Huang CY.
    Hum Reprod; 2006 Aug 17; 21(8):2175-9. PubMed ID: 16772284
    [Abstract] [Full Text] [Related]

  • 11. Strategies for the isolation and detection of fetal cells in transcervical samples.
    Bussani C, Cioni R, Scarselli B, Barciulli F, Bucciantini S, Simi P, Fogli A, Scarselli G.
    Prenat Diagn; 2002 Dec 17; 22(12):1098-101. PubMed ID: 12454965
    [Abstract] [Full Text] [Related]

  • 12. Prenatally detected trisomy 20 mosaicism.
    Robinson WP, McGillivray B, Lewis ME, Arbour L, Barrett I, Kalousek DK.
    Prenat Diagn; 2005 Mar 17; 25(3):239-44. PubMed ID: 15791659
    [Abstract] [Full Text] [Related]

  • 13. Screening for trisomy 18 by maternal age, fetal nuchal translucency, free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A.
    Kagan KO, Wright D, Maiz N, Pandeva I, Nicolaides KH.
    Ultrasound Obstet Gynecol; 2008 Sep 17; 32(4):488-92. PubMed ID: 18726925
    [Abstract] [Full Text] [Related]

  • 14. Real-time quantitative PCR for the detection of fetal aneuploidies.
    Zimmermann BG, Dudarewicz L.
    Methods Mol Biol; 2008 Sep 17; 444():95-109. PubMed ID: 18425474
    [Abstract] [Full Text] [Related]

  • 15. Human chromosome 21-specific DNA markers are useful in prenatal detection of Down syndrome.
    Liou JD, Chu DC, Cheng PJ, Chang SD, Sun CF, Wu YC, Liou WY, Chiu DT.
    Ann Clin Lab Sci; 2004 Sep 17; 34(3):319-23. PubMed ID: 15487707
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis and outcome of congenital cytomegalovirus infection in twin pregnancies.
    Yinon Y, Yagel S, Tepperberg-Dikawa M, Feldman B, Schiff E, Lipitz S.
    BJOG; 2006 Mar 17; 113(3):295-300. PubMed ID: 16487201
    [Abstract] [Full Text] [Related]

  • 17. [Detection of fetal short tandem repeat genotype in maternal plasma by multiplex fluorescent polymerase chain reaction].
    Liu FM, Feng X, Wang XY, Wang W, Ye YX, Chen H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec 17; 22(6):684-6. PubMed ID: 16331573
    [Abstract] [Full Text] [Related]

  • 18. Noninvasive genotyping of 9 Y-chromosome specific STR loci using circulatory fetal DNA in maternal plasma by multiplex PCR.
    Deng Z, Wu G, Li Q, Zhang X, Liang Y, Li D, Gao S, Lan Y.
    Prenat Diagn; 2006 Apr 17; 26(4):362-8. PubMed ID: 16566058
    [Abstract] [Full Text] [Related]

  • 19. [Prenatal gene diagnosis of paternally inherited alpha-thalassemia by detecting fetal DNA in maternal plasma].
    Chen P, Li MJ, Li MQ, Li SQ, Zhou LY, Lin WX.
    Zhonghua Yi Xue Za Zhi; 2007 Jun 12; 87(22):1540-4. PubMed ID: 17785106
    [Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second-trimester amniocenteses.
    Leung WC, Waters JJ, Chitty L.
    Prenat Diagn; 2004 Oct 12; 24(10):790-5. PubMed ID: 15503279
    [Abstract] [Full Text] [Related]

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