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1014 related items for PubMed ID: 16167939

  • 1. The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testing.
    Ogilvie CM, Lashwood A, Chitty L, Waters JJ, Scriven PN, Flinter F.
    BJOG; 2005 Oct; 112(10):1369-75. PubMed ID: 16167939
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  • 2. A retrospective evaluation of maternal serum screening for the detection of fetal aneuploidy.
    Suzumori K, Tanemura M, Murakami I, Okada S, Natori M, Tanaka M, Takagi T, Sato A.
    Prenat Diagn; 1997 Sep; 17(9):861-6. PubMed ID: 9316131
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  • 3. Fetuses with Down's Syndrome detected by prenatal screening are more likely to abort spontaneously than fetuses with Down's Syndrome not detected by prenatal screening.
    Leporrier N, Herrou M, Morello R, Leymarie P.
    BJOG; 2003 Jan; 110(1):18-21. PubMed ID: 12504930
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  • 6. Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening.
    Ryall RG, Callen D, Cocciolone R, Duvnjak A, Esca R, Frantzis N, Gjerde EM, Haan EA, Hocking T, Sutherland G, Thomas DW, Webb F.
    Prenat Diagn; 2001 Jul; 21(7):553-7. PubMed ID: 11494290
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  • 7. QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region.
    Hills A, Donaghue C, Waters J, Waters K, Sullivan C, Kulkarni A, Docherty Z, Mann K, Ogilvie CM.
    Prenat Diagn; 2010 Jun; 30(6):509-17. PubMed ID: 20509149
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  • 12. Comparison of Nicolaides' risk evaluation for Down's syndrome with a novel software: an analysis of 1,463 cases.
    Schmidt P, Staboulidou I, Soergel P, Wüstemann M, Hillemanns P, Scharf A.
    Arch Gynecol Obstet; 2007 Jun; 275(6):469-74. PubMed ID: 17333228
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  • 13. Pregnancy outcomes in unselected singleton pregnant women with an increased risk of first-trimester Down's syndrome.
    Liu SS, Lee FK, Lee JL, Tsai MS, Cheong ML, She BQ, Chen SC.
    Acta Obstet Gynecol Scand; 2004 Dec; 83(12):1130-4. PubMed ID: 15548144
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  • 14. Prenatal diagnosis of sex chromosome abnormalities: the 8-year experience of a single medical center.
    Vaknin Z, Reish O, Ben-Ami I, Heyman E, Herman A, Maymon R.
    Fetal Diagn Ther; 2008 Dec; 23(1):76-81. PubMed ID: 17934303
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  • 15. [Molecular biology usefulness for rapid diagnosis of Down's syndrome and common aneuploidies].
    Fauret AL, Bilan F, Patri S, Couet D, Marechaud M, Pierre F, Gilbert-Dussardier B, Kitzis A.
    Gynecol Obstet Fertil; 2009 Dec; 37(7-8):611-9. PubMed ID: 19574080
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  • 16. Full karyotyping, rapid aneuploidy diagnosis or both when invasive prenatal testing is performed for diagnosis of thalassaemia?
    Tse KY, Leung WC, Leung KY, Lee CP, Ng LK, Lau ET, Chan V, Tang MH.
    Mol Hum Reprod; 2006 Jan; 12(1):55-9. PubMed ID: 16421217
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  • 20. The impact of national guidance for anomaly screening and invasive testing: unintended consequences.
    Alberry M, Hassan WA, Goodburn S, Brockelsby J, Wladimiroff J, Nash R, Lees C.
    Arch Dis Child Fetal Neonatal Ed; 2014 Jan; 99(1):F83-6. PubMed ID: 23833074
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