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Journal Abstract Search

337 related items for PubMed ID: 9557898

  • 1. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
    Reish O, Wolach B, Amiel A, Kedar I, Dolfin T, Fejgin M.
    Am J Med Genet; 1998 Apr 28; 77(1):72-5. PubMed ID: 9557898
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of trisomy 3 mosaicism.
    Zaslav AL, Pierno G, Davis J, Fougner A, Jacob J, Kazi R, Blumenthal D, Sturim S, Shaham M, Fox J.
    Prenat Diagn; 2004 Sep 28; 24(9):693-6. PubMed ID: 15386452
    [Abstract] [Full Text] [Related]

  • 3. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
    Chen CP, Chern SR, Lee CC, Chang TY, Wang W, Tzen CY.
    Prenat Diagn; 2004 Jan 28; 24(1):38-44. PubMed ID: 14755408
    [Abstract] [Full Text] [Related]

  • 4. Amniotic trisomy 11 mosaicism--is it a benign finding?
    Basel-Vanagaite L, Davidov B, Friedman J, Yeshaya Y, Magal N, Drasinover V, Shohat M.
    Prenat Diagn; 2006 Sep 28; 26(9):778-81. PubMed ID: 16810710
    [Abstract] [Full Text] [Related]

  • 5. A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism.
    Von Beust G, Bartels I, Zoll B.
    Genet Couns; 2003 Sep 28; 14(1):67-74. PubMed ID: 12725591
    [Abstract] [Full Text] [Related]

  • 6. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S.
    Prenat Diagn; 1996 Oct 28; 16(10):893-7. PubMed ID: 8938057
    [Abstract] [Full Text] [Related]

  • 7. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
    Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G.
    Eur J Hum Genet; 1999 Oct 28; 7(4):421-6. PubMed ID: 10352932
    [Abstract] [Full Text] [Related]

  • 8. Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.
    Font-Montgomery E, Stone KM, Weaver DD, Vance GH, Das S, Thurston VC.
    Birth Defects Res A Clin Mol Teratol; 2005 Aug 28; 73(8):577-82. PubMed ID: 16007591
    [Abstract] [Full Text] [Related]

  • 9. Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy.
    Chen M, Yeh GP, Shih JC, Wang BT.
    Prenat Diagn; 2004 Feb 28; 24(2):137-43. PubMed ID: 14974123
    [Abstract] [Full Text] [Related]

  • 10. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism.
    Langlois S, Yong PJ, Yong SL, Barrett I, Kalousek DK, Miny P, Exeler R, Morris K, Robinson WP.
    Prenat Diagn; 2006 Jun 28; 26(6):548-58. PubMed ID: 16683298
    [Abstract] [Full Text] [Related]

  • 11. Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues.
    Morales C, Cuatrecasas E, Mademont-Soler I, Clusellas N, Peruga E, Català V, Garrido C, Milà M, Soler A, Sánchez A.
    Eur J Med Genet; 2010 Jun 28; 53(4):197-200. PubMed ID: 20350623
    [Abstract] [Full Text] [Related]

  • 12. A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.
    Roberts E, Dunlop J, Davis GS, Churchill D, Davison EV.
    Prenat Diagn; 2003 Jul 28; 23(7):564-5. PubMed ID: 12868084
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May 28; 25(5):354-7. PubMed ID: 15906424
    [Abstract] [Full Text] [Related]

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  • 15. Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.
    Velissariou V, Antoniadi T, Gyftodimou J, Bakou K, Grigoriadou M, Christopoulou S, Hatzipouliou A, Donoghue J, Karatzis P, Katsarou E, Petersen MB.
    Eur J Hum Genet; 2002 Nov 28; 10(11):694-8. PubMed ID: 12404100
    [Abstract] [Full Text] [Related]

  • 16. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
    Kosaki R, Hanai S, Kakishima H, Okada MA, Hayashi S, Ito Y, Takahashi T, Kosaki K, Okuyama T.
    Congenit Anom (Kyoto); 2006 Jun 28; 46(2):115-7. PubMed ID: 16732770
    [Abstract] [Full Text] [Related]

  • 17. Trisomy 12/monosomy X/normal female mosaicism: prenatal detection and confirmation in a liveborn.
    Spiro R, Rita D, Jazmines L, Jones C, Booth CW.
    Prenat Diagn; 1996 Aug 28; 16(8):734-40. PubMed ID: 8878284
    [Abstract] [Full Text] [Related]

  • 18. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
    Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G.
    Prenat Diagn; 2003 Feb 28; 23(2):128-33. PubMed ID: 12575019
    [Abstract] [Full Text] [Related]

  • 19. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
    Chen CP, Su YN, Su JW, Chern SR, Chen YT, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Mar 28; 52(1):97-105. PubMed ID: 23548227
    [Abstract] [Full Text] [Related]

  • 20. [Intrauterine growth retardation associated with a mosaic trisomy 20 limited to the placenta. A case report].
    Lacoste-Jugnet N, Depret-Mosser S, Vinatier D, Savary D, Dufour P, Lefebvre-Maunoury C, Monnier JC.
    J Gynecol Obstet Biol Reprod (Paris); 1995 Mar 28; 24(6):606-9. PubMed ID: 8830080
    [Abstract] [Full Text] [Related]

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