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Journal Abstract Search

375 related items for PubMed ID: 12975788

  • 1. 22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signs.
    Volpe P, Marasini M, Caruso G, Marzullo A, Buonadonna AL, Arciprete P, Di Paolo S, Volpe G, Gentile M.
    Prenat Diagn; 2003 Sep; 23(9):752-7. PubMed ID: 12975788
    [Abstract] [Full Text] [Related]

  • 2. Fetal interrupted aortic arch: 2D-4D echocardiography, associations and outcome.
    Volpe P, Tuo G, De Robertis V, Campobasso G, Marasini M, Tempesta A, Gentile M, Rembouskos G.
    Ultrasound Obstet Gynecol; 2010 Mar; 35(3):302-9. PubMed ID: 20069674
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  • 3. Prenatal diagnosis of interruption of the aortic arch and its association with deletion of chromosome 22q11.
    Volpe P, Marasini M, Caruso G, Gentile M.
    Ultrasound Obstet Gynecol; 2002 Oct; 20(4):327-31. PubMed ID: 12383312
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  • 4. Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects.
    Chaoui R, Kalache KD, Heling KS, Tennstedt C, Bommer C, Körner H.
    Ultrasound Obstet Gynecol; 2002 Dec; 20(6):546-52. PubMed ID: 12493042
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  • 5. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D, Engels H, Bauriedel G, Wiebe W, Schwanitz G.
    Dtsch Med Wochenschr; 1999 Jan 08; 124(1-2):3-7. PubMed ID: 9951451
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  • 6. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
    Webber SA, Hatchwell E, Barber JC, Daubeney PE, Crolla JA, Salmon AP, Keeton BR, Temple IK, Dennis NR.
    J Pediatr; 1996 Jul 08; 129(1):26-32. PubMed ID: 8757559
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  • 7. [Prenatally detected aortic arch anomalies and their consequences after birth].
    Tidrenczel Z, P Tardy E, Ladányi A, Hajdú J, Böjtös I, Sarkadi E, Simon J, Demeter J.
    Orv Hetil; 2023 Jul 16; 164(28):1111-1120. PubMed ID: 37454329
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, Wu PS, Chen YT, Chang SY.
    Taiwan J Obstet Gynecol; 2014 Jun 16; 53(2):248-51. PubMed ID: 25017279
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  • 14. Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
    Bretelle F, Beyer L, Pellissier MC, Missirian C, Sigaudy S, Gamerre M, D'Ercole C, Philip N.
    Eur J Med Genet; 2010 Jun 16; 53(6):367-70. PubMed ID: 20659598
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  • 16. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M, Hwu WL, Kuo SJ, Chen CP, Yin PL, Chang SP, Lee DJ, Chen TH, Wang BT, Lin CC.
    Ultrasound Obstet Gynecol; 2006 Dec 16; 28(7):939-43. PubMed ID: 17121426
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  • 18. Prenatal diagnosis and outcome of right aortic arch without significant intracardiac anomaly.
    Razon Y, Berant M, Fogelman R, Amir G, Birk E.
    J Am Soc Echocardiogr; 2014 Dec 16; 27(12):1352-8. PubMed ID: 25240492
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  • 19. Use of amniocytes for prenatal diagnosis of 22q11.2 microdeletion syndrome: a feasibility study.
    Liu T, Liu Q, Wang YX, Yang D, Xin Y, Fang Z, Ding SF, Yang JF.
    Chin Med J (Engl); 2010 Feb 20; 123(4):438-42. PubMed ID: 20193483
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