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Journal Abstract Search

254 related items for PubMed ID: 3055033

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  • 3. Prenatal cytogenetic diagnosis. Amniotic cell culture versus chorionic villus sampling.
    Bell JA, Pearn JH, Smith A.
    Med J Aust; 1987 Jan 05; 146(1):27-9. PubMed ID: 3796391
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  • 4. Prenatal cytogenetic diagnosis--a current audit. A review of 2000 cases of prenatal cytogenetic diagnoses after amniocentesis, and comparisons with early experience.
    Bell JA, Pearn JH, Wilson BH, Ansford AJ.
    Med J Aust; 1987 Jan 05; 146(1):12-5. PubMed ID: 3796389
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  • 5. Early sonographically guided amniocenteses with filtration technique: follow-up on 249 procedures.
    Sundberg K, Bang J, Brocks V, Jensen FR, Smidt-Jensen S, Philip J.
    J Ultrasound Med; 1995 Aug 05; 14(8):585-90. PubMed ID: 7474056
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  • 6. Prenatal diagnosis in twin gestations: a comparison between second-trimester amniocentesis and first-trimester chorionic villus sampling.
    Wapner RJ, Johnson A, Davis G, Urban A, Morgan P, Jackson L.
    Obstet Gynecol; 1993 Jul 05; 82(1):49-56. PubMed ID: 8515925
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  • 7. Amniocentesis before 14 completed weeks as an alternative to transabdominal chorionic villus sampling: a controlled trial with infant follow-up.
    Nagel HT, Vandenbussche FP, Keirse MJ, Oepkes D, Oosterwijk JC, Beverstock G, Kanhai HH.
    Prenat Diagn; 1998 May 05; 18(5):465-75. PubMed ID: 9621380
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  • 8. [Early amniocentesis for cytogenetic diagnosis].
    Lindner C, Hüneke B, Masson D, Schlotfeldt T, Kerber S, Held KR.
    Geburtshilfe Frauenheilkd; 1990 Dec 05; 50(12):954-8. PubMed ID: 1707842
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  • 9. [Amniocentesis indications and diagnostics].
    Barrelet V, Wilson E, Weihs D, Cruz J.
    Rev Med Suisse Romande; 1974 Oct 05; 94(10):793-802. PubMed ID: 4438866
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  • 10. [The diagnostic potential of amniocentesis in the first 12 weeks of pregnancy].
    Bartosch B, Klein M, Beck A, Schnedl W.
    Geburtshilfe Frauenheilkd; 1991 Nov 05; 51(11):886-9. PubMed ID: 1773923
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  • 11. Use of ultrasound for placental localization in genetic amniocentesis.
    Miskin M, Doran TA, Rudd N, Gardner HA, Liedgren S, Benzie R.
    Obstet Gynecol; 1974 Jun 05; 43(6):872-7. PubMed ID: 4829282
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  • 12. Early amniocentesis: report of 407 cases with neonatal follow-up.
    Penso CA, Sandstrom MM, Garber MF, Ladoulis M, Stryker JM, Benacerraf BB.
    Obstet Gynecol; 1990 Dec 05; 76(6):1032-6. PubMed ID: 2234711
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  • 13. Risk of fetal chromosomal anomalies in patients with elevated maternal serum alpha-fetoprotein.
    Warner AA, Pettenati MJ, Burton BK.
    Obstet Gynecol; 1990 Jan 05; 75(1):64-6. PubMed ID: 1688649
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  • 14. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP, Wu JP, Li XT, Lei CX, Xu JZ, Yin M.
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep 05; 46(9):644-8. PubMed ID: 22176986
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  • 15. Early filtration amniocentesis for further investigation of mosaicism diagnosed by chorionic villus sampling.
    Sundberg K, Lundsteen C, Philip J.
    Prenat Diagn; 1996 Dec 05; 16(12):1121-7. PubMed ID: 8994248
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  • 20. Prenatal diagnosis of genetic disease in Canada: report of a collaborative study.
    Simpson NE, Dallaire L, Miller JR, Siminovich L, Hamerton JL, Miller J, McKeen C.
    Can Med Assoc J; 1976 Oct 23; 115(8):739-48. PubMed ID: 61796
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