These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

311 related items for PubMed ID: 19816033

  • 1. Increased fetal nuchal translucency as a sole clue in the prenatal diagnosis of a fetus with trisomy 13.
    Ki KD, Kim SR, Lee WI.
    Fetal Diagn Ther; 2009; 26(1):54-6. PubMed ID: 19816033
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. First-trimester ultrasonographic screening for trisomy 21 using fetal nuchal translucency and nasal bone.
    Sepulveda W, Wong AE, Dezerega V.
    Obstet Gynecol; 2007 May; 109(5):1040-5. PubMed ID: 17470580
    [Abstract] [Full Text] [Related]

  • 4. Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling.
    Molina-Gomes D, Nebout V, Daikha-Dahmane F, Vialard F, Ville Y, Selva J.
    Prenat Diagn; 2006 Mar; 26(3):239-41. PubMed ID: 16485319
    [Abstract] [Full Text] [Related]

  • 5. 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; 26(10):917-9. PubMed ID: 16845680
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [Abstract] [Full Text] [Related]

  • 9. Association of fetal choroid plexus cysts with trisomy 18 in a population previously screened by nuchal translucency thickness measurement.
    Cheng PJ, Shaw SW, Soong YK.
    J Soc Gynecol Investig; 2006 May; 13(4):280-4. PubMed ID: 16697944
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. 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]

  • 13. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
    Chen CP, Su YN, Tsai FJ, Lin MH, Wu PC, Chern SR, Lee CC, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
    [Abstract] [Full Text] [Related]

  • 14. Prenatal sonographic features of trisomy 1q.
    Wax JR, Carpenter M, Chard R, Cartin A, Pinette MG, Blackstone J.
    J Clin Ultrasound; 2008 May; 36(4):231-6. PubMed ID: 17661383
    [Abstract] [Full Text] [Related]

  • 15. Diagnosis and prediction of parental origin of triploidies by fetal nuchal translucency and maternal serum free beta-hCG and PAPP-A at 11-14 weeks of gestation.
    Barken SS, Skibsted L, Jensen LN, Sperling L, Zingenberg H, Brøndum-Nielsen K.
    Acta Obstet Gynecol Scand; 2008 May; 87(9):975-8. PubMed ID: 18720036
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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]

  • 18. Prenatal diagnosis of complete sole trisomy 1q.
    Pettenati MJ, Berry M, Shashi V, Hartley Bowen J, Harper M.
    Prenat Diagn; 2001 Jun; 21(6):435-40. PubMed ID: 11438944
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
    Santolaya-Forgas J, De Leon J, Powell WC, Tonk V.
    Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.