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94 related items for PubMed ID: 15712327

  • 1. Prenatal diagnosis of trisomy 18: report of 30 cases.
    Yang JH, Chung JH, Shin JS, Choi JS, Ryu HM, Kim MY.
    Prenat Diagn; 2005 Feb; 25(2):119-22. PubMed ID: 15712327
    [Abstract] [Full Text] [Related]

  • 2. [The prenatal detection of trisomy 13, 18, and 21: comparison of the advanced first trimester screening (AFS) with the first trimester screening according to Nicolaides].
    Hörmansdörfer C, Schmidt P, Hillemanns P, Scharf A.
    Z Geburtshilfe Neonatol; 2007 Dec; 211(6):243-9. PubMed ID: 18176905
    [Abstract] [Full Text] [Related]

  • 3. Multicenter study of first-trimester screening for trisomy 21 in 75 821 pregnancies: results and estimation of the potential impact of individual risk-orientated two-stage first-trimester screening.
    Nicolaides KH, Spencer K, Avgidou K, Faiola S, Falcon O.
    Ultrasound Obstet Gynecol; 2005 Mar; 25(3):221-6. PubMed ID: 15736186
    [Abstract] [Full Text] [Related]

  • 4. Screening for trisomy 21 by fetal tricuspid regurgitation, nuchal translucency and maternal serum free beta-hCG and PAPP-A at 11 + 0 to 13 + 6 weeks.
    Falcon O, Auer M, Gerovassili A, Spencer K, Nicolaides KH.
    Ultrasound Obstet Gynecol; 2006 Feb; 27(2):151-5. PubMed ID: 16388509
    [Abstract] [Full Text] [Related]

  • 5. Prenatal ultrasound findings in complete trisomy 9.
    Sepulveda W, Wimalasundera RC, Taylor MJ, Blunt S, Be C, De La Fuente S.
    Ultrasound Obstet Gynecol; 2003 Nov; 22(5):479-83. PubMed ID: 14618660
    [Abstract] [Full Text] [Related]

  • 6. Second trimester prenatal ultrasound for the detection of pregnancies at increased risk of Trisomy 18 based on serum screening.
    Cho RC, Chu P, Smith-Bindman R.
    Prenat Diagn; 2009 Feb; 29(2):129-39. PubMed ID: 19142904
    [Abstract] [Full Text] [Related]

  • 7. 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; 32(4):488-92. PubMed ID: 18726925
    [Abstract] [Full Text] [Related]

  • 8. Trisomy 13 and trisomy 18 in a defined population: epidemiological, genetic and prenatal observations.
    Parker MJ, Budd JL, Draper ES, Young ID.
    Prenat Diagn; 2003 Oct; 23(10):856-60. PubMed ID: 14558033
    [Abstract] [Full Text] [Related]

  • 9. Performance of first-trimester combined screening for trisomy 13 and 18 with the double test taken at a gestational age of 8 + 0 to 13 + 6.
    Kirkegaard I, Petersen OB, Uldbjerg N, Tørring N.
    Prenat Diagn; 2009 Jun; 29(6):582-7. PubMed ID: 19288457
    [Abstract] [Full Text] [Related]

  • 10. Is ultrasound alone enough for prenatal screening of trisomy 18? A single centre experience in 69 cases over 10 years.
    Lai S, Lau WL, Leung WC, Lai FK, Chin R.
    Prenat Diagn; 2010 Nov; 30(11):1094-9. PubMed ID: 20925041
    [Abstract] [Full Text] [Related]

  • 11. Sonographic screening for trisomy 13 at 11 to 13(+6) weeks of gestation.
    Papageorghiou AT, Avgidou K, Spencer K, Nix B, Nicolaides KH.
    Am J Obstet Gynecol; 2006 Feb; 194(2):397-401. PubMed ID: 16458636
    [Abstract] [Full Text] [Related]

  • 12. The utility of detailed first trimester ultrasound examination in abnormal fetal nuchal translucency.
    Bronshtein M, Zimmer EZ, Blazer S.
    Prenat Diagn; 2008 Nov; 28(11):1037-41. PubMed ID: 18925580
    [Abstract] [Full Text] [Related]

  • 13. If nuchal translucency screening is combined with first-trimester serum screening the need for fetal karyotyping decreases.
    Marsk A, Grunewald C, Saltvedt S, Valentin L, Almström H.
    Acta Obstet Gynecol Scand; 2006 Nov; 85(5):534-8. PubMed ID: 16752230
    [Abstract] [Full Text] [Related]

  • 14. Screening for trisomies 21, 18 and 13 by maternal age, fetal nuchal translucency, fetal heart rate, free beta-hCG and pregnancy-associated plasma protein-A.
    Kagan KO, Wright D, Valencia C, Maiz N, Nicolaides KH.
    Hum Reprod; 2008 Sep; 23(9):1968-75. PubMed ID: 18544579
    [Abstract] [Full Text] [Related]

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

  • 16. The association between an abnormal nuchal skin fold, trisomy 21, and ultrasound abnormalities identified during the second trimester of pregnancy.
    DeVore GR, Alfi O.
    Ultrasound Obstet Gynecol; 1993 Nov 01; 3(6):387-94. PubMed ID: 12797239
    [Abstract] [Full Text] [Related]

  • 17. Chorionic villus sampling for early prenatal diagnosis at Bhumibol Adulyadej Hospital.
    Rueangchainikhom W, Sarapak S, Orungrote N.
    J Med Assoc Thai; 2008 Jan 01; 91(1):1-6. PubMed ID: 18386536
    [Abstract] [Full Text] [Related]

  • 18. Uptake of invasive prenatal diagnostic tests in women after detection of soft markers for chromosomal abnormality on ultrasonographic evaluation.
    Sharda S, Phadke SR.
    J Perinatol; 2007 Sep 01; 27(9):550-5. PubMed ID: 17611609
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 107(4):877-9. PubMed ID: 16582126
    [Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of a partial 6q trisomy: a case report.
    Valerio D, Di Domenico A, Felicetti M, La Boccetta A, Ferrara C, Antonio N, Borrelli AL.
    Prenat Diagn; 2006 Oct 01; 26(10):917-9. PubMed ID: 16845680
    [Abstract] [Full Text] [Related]

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