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Journal Abstract Search

145 related items for PubMed ID: 17074451

  • 1. Quality control of prenatal sonography in detecting trisomy 18. The value of perinatal autopsy.
    Szigeti Z, Csapó Z, Joó J, Pete B, Papp Z, Papp C.
    Early Hum Dev; 2007 Aug; 83(8):505-9. PubMed ID: 17074451
    [Abstract] [Full Text] [Related]

  • 2. Correlation of prenatal ultrasound diagnosis and pathologic findings in fetuses with trisomy 13.
    Szigeti Z, Csapó Z, Joó JG, Pete B, Papp Z, Papp C.
    Prenat Diagn; 2006 Dec; 26(13):1262-6. PubMed ID: 17099926
    [Abstract] [Full Text] [Related]

  • 3. The role of perinatal autopsy in the management of pregnancies with major fetal trisomies.
    Papp C, Szigeti Z, Joó JG, Tóth-Pál E, Hajdú J, Papp Z.
    Pathol Res Pract; 2007 Dec; 203(7):525-31. PubMed ID: 17574347
    [Abstract] [Full Text] [Related]

  • 4. Correlation of prenatal sonographic diagnosis and morphologic findings of fetal autopsy in fetuses with trisomy 21.
    Szigeti Z, Csaba A, Pete B, Hajdú J, Papp Z, Papp C.
    J Ultrasound Med; 2007 Jan; 26(1):61-8; quiz 69-70. PubMed ID: 17182710
    [Abstract] [Full Text] [Related]

  • 5. Value of a complete sonographic survey in detecting fetal abnormalities: correlation with perinatal autopsy.
    Yeo L, Guzman ER, Shen-Schwarz S, Walters C, Vintzileos AM.
    J Ultrasound Med; 2002 May; 21(5):501-10. PubMed ID: 12008812
    [Abstract] [Full Text] [Related]

  • 6. Prenatal detection of fetal trisomy 18 through abnormal sonographic features.
    Yeo L, Guzman ER, Day-Salvatore D, Walters C, Chavez D, Vintzileos AM.
    J Ultrasound Med; 2003 Jun; 22(6):581-90; quiz 591-2. PubMed ID: 12807074
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of craniomaxillofacial malformations: a characterization of phenotypes in trisomies 13, 18, and 21 by ultrasound and pathology.
    Ettema AM, Wenghoefer M, Hansmann M, Carels CE, Borstlap WA, Bergé SJ.
    Cleft Palate Craniofac J; 2010 Mar; 47(2):189-96. PubMed ID: 19860526
    [Abstract] [Full Text] [Related]

  • 8. Phenotypic expression in the first case of complete trisomy 12: combination of prenatal ultrasound and necropsic examination.
    Machado AP, Ramalho C, Loureiro T, Cunha M, Dória S, Carvalho F, Oliveira JP, Brandão O, Matias A.
    Fetal Diagn Ther; 2009 Mar; 25(2):234-8. PubMed ID: 19494495
    [Abstract] [Full Text] [Related]

  • 9. Evaluating the incidence and likelihood ratios for chromosomal abnormalities in fetuses with common central nervous system malformations.
    Goetzinger KR, Stamilio DM, Dicke JM, Macones GA, Odibo AO.
    Am J Obstet Gynecol; 2008 Sep; 199(3):285.e1-6. PubMed ID: 18771985
    [Abstract] [Full Text] [Related]

  • 10. Comparison of prenatal ultrasound and postmortem findings in fetuses and infants with central nervous system anomalies.
    Isaksen CV, Eik-Nes SH, Blaas HG, Torp SH.
    Ultrasound Obstet Gynecol; 1998 Apr; 11(4):246-53. PubMed ID: 9618846
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of complete trisomy 19q.
    Babić I, Brajenović-Milić B, Petrović O, Mustać E, Kapović M.
    Prenat Diagn; 2007 Jul; 27(7):644-7. PubMed ID: 17437325
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Trisomy 13 syndrome: prenatal US findings in a review of 33 cases.
    Lehman CD, Nyberg DA, Winter TC, Kapur RP, Resta RG, Luthy DA.
    Radiology; 1995 Jan; 194(1):217-22. PubMed ID: 7997556
    [Abstract] [Full Text] [Related]

  • 14. 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 Jan; 26(1):54-6. PubMed ID: 19816033
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
    [Abstract] [Full Text] [Related]

  • 17. [Value of fetopathological examination in medical abortions: comparison of prenatal diagnosis and autopsy results of 300 fetuses].
    Laussel-Riera A, Devisme L, Manouvrier-Hanu S, Puech F, Robert Y, Gosselin B.
    Ann Pathol; 2000 Dec; 20(6):549-57. PubMed ID: 11148350
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of trisomy 9.
    Nakagawa M, Hashimoto K, Ohira H, Hamanaka T, Ozaki M, Suehara N.
    Fetal Diagn Ther; 2006 Dec; 21(1):68-71. PubMed ID: 16354979
    [Abstract] [Full Text] [Related]

  • 19. Karyotyping for isolated neural tube defects. A report of two cases.
    O'Reilly GC, Shields LE.
    J Reprod Med; 2000 Nov; 45(11):950-2. PubMed ID: 11127112
    [Abstract] [Full Text] [Related]

  • 20. Prenatal sonographic findings of trisomy 18: review of 47 cases.
    Nyberg DA, Kramer D, Resta RG, Kapur R, Mahony BS, Luthy DA, Hickok D.
    J Ultrasound Med; 1993 Feb; 12(2):103-13. PubMed ID: 8468736
    [Abstract] [Full Text] [Related]

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