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Journal Abstract Search

150 related items for PubMed ID: 19127784

  • 1. Prenatal ultrasonographic findings in "trisomy 13".
    Pitukkijronnakorn S, Promsonthi P, Panburana P, Rangsiprakarn R, Chittacharoen A.
    J Med Assoc Thai; 2008 Nov; 91(11):1651-5. PubMed ID: 19127784
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. [Study on key techniques and intervention in reducing birth defects].
    Zhu BS, Su J, Lu XH, He J, Zhu S, Jiao CX, Zhang JM, Tang XH, Tao Y, Lin KP, Chen H, Li SY.
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):658-63. PubMed ID: 22176989
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Prenatal diagnosis of trisomy 13: analysis of 28 cases.
    Papp C, Beke A, Ban Z, Szigeti Z, Toth-Pal E, Papp Z.
    J Ultrasound Med; 2006 Apr; 25(4):429-35. PubMed ID: 16567430
    [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. [The prenatal detection of trisomy 13, 18, and 21: comparison of the advanced first trimester screening (AFS) with the first trimester screening according to Nicolaides].
    Hörmansdörfer C, Schmidt P, Hillemanns P, Scharf A.
    Z Geburtshilfe Neonatol; 2007 Dec; 211(6):243-9. PubMed ID: 18176905
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report.
    Phadke SR, Thakur S.
    Prenat Diagn; 2002 Dec; 22(13):1240-1. PubMed ID: 12478643
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.
    Corsello G, Buttitta P, Cammarata M, Lo Presti A, Maresi E, Zumpani L, Giuffrè L.
    Am J Med Genet; 1990 Oct; 37(2):244-9. PubMed ID: 2147361
    [Abstract] [Full Text] [Related]

  • 11. Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.
    Sergi C, Gekas J, Kamnasaran D.
    Fetal Pediatr Pathol; 2012 Oct; 31(5):315-8. PubMed ID: 22432933
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP, Devriendt K, Lee CC, Chen WL, Wang W, Wang TY.
    Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?
    Karmous-Benailly H, Tabet AC, Thaly A, Dupuy O, Huten Y, Luton D, Baumann C, Delezoide AL.
    Prenat Diagn; 2005 Mar; 25(3):193-7. PubMed ID: 15791668
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
    Chen CP, Chern SR, Hsu CY, Lee CC, Lee MS, Wang W.
    Prenat Diagn; 2005 Apr; 25(4):334-6. PubMed ID: 15849788
    [No Abstract] [Full Text] [Related]

  • 15. [Prenatal diagnosis of trisomy 13 and trisomy 18: the experience of Assaf-Harofe Medical Center].
    Naor Dovev M, Maymon R, Keidar R, Reish O, Melcer Y, Vaknin Z.
    Harefuah; 2014 Aug; 153(8):453-7, 499, 498. PubMed ID: 25286634
    [Abstract] [Full Text] [Related]

  • 16. Chromosomal abnormalities in fetuses with open neural tube defects: prenatal identification with ultrasound.
    Sepulveda W, Corral E, Ayala C, Be C, Gutierrez J, Vasquez P.
    Ultrasound Obstet Gynecol; 2004 Apr; 23(4):352-6. PubMed ID: 15065184
    [Abstract] [Full Text] [Related]

  • 17. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
    Pires A, Ramos L, Venâncio M, Rei AI, Castedo S, Saraiva J.
    Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
    [Abstract] [Full Text] [Related]

  • 18. Cyclopia, proboscis and alobar holoprosencephaly representative for trisomy 13.
    Bozkurt O, Kanmaz HG, Sahin S, Canpolat FE, Uras N, Oguz SS, Dilmen U.
    Genet Couns; 2014 Apr; 25(3):349-51. PubMed ID: 25365860
    [No Abstract] [Full Text] [Related]

  • 19. Antenatally detectable markers for the diagnosis of autosomally trisomic fetuses in at-risk pregnancies.
    Salihu HM, Boos R, Schmidt W.
    Am J Perinatol; 1997 May; 14(5):257-61. PubMed ID: 9259939
    [Abstract] [Full Text] [Related]

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

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