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Journal Abstract Search

241 related items for PubMed ID: 1741869

  • 1. Management of prenatally detected nonlethal fetal anomalies: is a karyotype of benefit?
    Brumfield CG, Davis RO, Hauth JC, Cosper P, Colvin EV, Finley SC.
    Am J Perinatol; 1991 Jul; 8(4):255-8. PubMed ID: 1741869
    [Abstract] [Full Text] [Related]

  • 2. Karyotype abnormalities in fetuses diagnosed as abnormal on ultrasound before 20 weeks' gestational age.
    Halliday J, Lumley J, Bankier A.
    Prenat Diagn; 1994 Aug; 14(8):689-97. PubMed ID: 7991511
    [Abstract] [Full Text] [Related]

  • 3. Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.
    Colvin J, Bower C, Dickinson JE, Sokol J.
    Pediatrics; 2005 Sep; 116(3):e356-63. PubMed ID: 16140678
    [Abstract] [Full Text] [Related]

  • 4. Fetal omphalocele detected early in pregnancy: associated anomalies and outcomes.
    Blazer S, Zimmer EZ, Gover A, Bronshtein M.
    Radiology; 2004 Jul; 232(1):191-5. PubMed ID: 15220502
    [Abstract] [Full Text] [Related]

  • 5. Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study.
    Wilson RD, Chitayat D, McGillivray BC.
    Am J Med Genet; 1992 Nov 15; 44(5):586-90. PubMed ID: 1481814
    [Abstract] [Full Text] [Related]

  • 6. Fetal outcome in nuchal translucency with emphasis on normal fetal karyotype.
    Cha'ban FK, Van Splunder P, Los FJ, Wladimiroff JW.
    Prenat Diagn; 1996 Jun 15; 16(6):537-41. PubMed ID: 8809895
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis and management of congenital heart defect: significance of associated fetal anomalies and prenatal chromosome studies.
    Wladimiroff JW, Stewart PA, Sachs ES, Niermeijer MF.
    Am J Med Genet; 1985 Jun 15; 21(2):285-90. PubMed ID: 3893127
    [Abstract] [Full Text] [Related]

  • 8. Abnormal pregnancy sonogram: selective indication for fetal karyotype.
    Williamson RA, Weiner CP, Patil S, Benda J, Varner MW, Abu-Yousef MM.
    Obstet Gynecol; 1987 Jan 15; 69(1):15-20. PubMed ID: 3540760
    [Abstract] [Full Text] [Related]

  • 9. Fetal and placenta chromosome constitution in 237 pregnancy losses.
    Baena N, Guitart M, Ferreres JC, Gabau E, Corona M, Mellado F, Egozcue J, Caballín MR.
    Ann Genet; 2001 Jan 15; 44(2):83-8. PubMed ID: 11522246
    [Abstract] [Full Text] [Related]

  • 10. [Karyotyping of fetuses with developmental disorders. A 5-year material 1985-89].
    Tuveng JM, Eik-Nes SH, Sviggum O, Isaksen C, Berg K, Leren TP, van der Hagen CB.
    Tidsskr Nor Laegeforen; 1993 Jan 30; 113(3):339-42. PubMed ID: 8441983
    [Abstract] [Full Text] [Related]

  • 11. The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities.
    Rhoads GG, Jackson LG, Schlesselman SE, de la Cruz FF, Desnick RJ, Golbus MS, Ledbetter DH, Lubs HA, Mahoney MJ, Pergament E.
    N Engl J Med; 1989 Mar 09; 320(10):609-17. PubMed ID: 2645520
    [Abstract] [Full Text] [Related]

  • 12. Is rapid aneuploidy screening used alone acceptable in prenatal diagnosis? An evaluation of the possible role of ultrasound examination.
    Gaudry P, Lebbar A, Choiset A, Girard S, Lewin F, Tsatsaris V, Grangé G.
    Fetal Diagn Ther; 2009 Mar 09; 25(2):285-90. PubMed ID: 19521096
    [Abstract] [Full Text] [Related]

  • 13. Pregnancy outcome in fetuses with increased nuchal translucency and normal karyotype.
    Senat MV, De Keersmaecker B, Audibert F, Montcharmont G, Frydman R, Ville Y.
    Prenat Diagn; 2002 May 09; 22(5):345-9. PubMed ID: 12001183
    [Abstract] [Full Text] [Related]

  • 14. Fetal karyotype following ascertainment of fetal anomalies by ultrasound.
    Palmer CG, Miles JH, Howard-Peebles PN, Magenis RE, Patil S, Friedman JM.
    Prenat Diagn; 1987 Oct 09; 7(8):551-5. PubMed ID: 3317386
    [Abstract] [Full Text] [Related]

  • 15. Role of amniocentesis in ultrasound-detected fetal malformations.
    Platt LD, DeVore GR, Lopez E, Herbert W, Falk R, Alfi O.
    Obstet Gynecol; 1986 Aug 09; 68(2):153-5. PubMed ID: 3526215
    [Abstract] [Full Text] [Related]

  • 16. [Usefulness of ultrasonographic markers in chromosomal abnormalities].
    Rivera Muñoz JE, Leis Márquez MT, García-Cavazos RJ, Hernández Andrade EA, Guzmán Huerta ME, Rodríguez-Bosch MR.
    Ginecol Obstet Mex; 1997 Sep 09; 65():394-9. PubMed ID: 9410812
    [Abstract] [Full Text] [Related]

  • 17. [Prenatal chromosome findings in sonographically conspicuous fetuses].
    Rezai K, Holzgreve W, Schloo R, Tercanli S, Horst J, Miny P.
    Geburtshilfe Frauenheilkd; 1991 Mar 09; 51(3):211-6. PubMed ID: 2055396
    [Abstract] [Full Text] [Related]

  • 18. A correlative study of prenatal ultrasound and post-mortem findings in fetuses and infants with an abnormal karyotype.
    Isaksen CV, Eik-Nes SH, Blaas HG, Torp SH, van der Hagen CB, Ormerod E.
    Ultrasound Obstet Gynecol; 2000 Jul 09; 16(1):37-45. PubMed ID: 11084963
    [Abstract] [Full Text] [Related]

  • 19. Characteristics and outcome of 90 cases of fetal omphalocele.
    Brantberg A, Blaas HG, Haugen SE, Eik-Nes SH.
    Ultrasound Obstet Gynecol; 2005 Oct 09; 26(5):527-37. PubMed ID: 16184512
    [Abstract] [Full Text] [Related]

  • 20. [Prenatal diagnosis by amniocentesis. Clinical and cytogenetic experience in 1,500 cases].
    Grether-González P, Cámara-Polanco V, Ulloa-Avilés V, Salas-Labadia C, Almanza-Márquez R, Kogan-Frenk S, Kuttothara A.
    Ginecol Obstet Mex; 2010 Sep 09; 78(9):493-503. PubMed ID: 21961367
    [Abstract] [Full Text] [Related]

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