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270 related items for PubMed ID: 11438954

  • 1. Complete karyotype discrepancy between placental and fetal cells in a case of ring chromosome 18.
    Fischer W, Dermitzel A, Osmers R, Pruggmayer M.
    Prenat Diagn; 2001 Jun; 21(6):481-3. PubMed ID: 11438954
    [Abstract] [Full Text] [Related]

  • 2. Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues.
    Hansson K, Poelma WM, Zondervan HA, Leschot NJ.
    Prenat Diagn; 1998 Sep; 18(9):975-8. PubMed ID: 9793985
    [Abstract] [Full Text] [Related]

  • 3. Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.
    Wegner RD, Schröck E, Obladen M, Becker R, Stumm M, Sperling K.
    Prenat Diagn; 1996 Aug; 16(8):741-8. PubMed ID: 8878285
    [Abstract] [Full Text] [Related]

  • 4. Discrepancy between the fetus and extra-embryonic tissues in prenatally detected mosaic distal 5p deletion.
    Chen CP, Lee CC, Town DD, Lee MS, Wang W.
    Genet Couns; 2004 Aug; 15(4):473-6. PubMed ID: 15658625
    [Abstract] [Full Text] [Related]

  • 5. Complete discrepancy between QF-PCR analysis of uncultured villi and karyotyping of cultured cells in the prenatal diagnosis of trisomy 21 in three CVS.
    Waters JJ, Mann K, Grimsley L, Ogilvie CM, Donaghue C, Staples L, Hills A, Adams T, Wilson C.
    Prenat Diagn; 2007 Apr; 27(4):332-9. PubMed ID: 17286305
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [Abstract] [Full Text] [Related]

  • 7. 46,XY,18q+/46,XY,18q- mosaicism in a fragile X prenatal diagnosis.
    Rodriguez-Revenga L, Badenas C, Madrigal I, Sánchez A, Soler A, Carrió A, Milà M.
    Prenat Diagn; 2005 Jun; 25(6):448-50. PubMed ID: 15966059
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes.
    Nucaro AL, Rossino R, Pruna D, Rassu S, Cianchetti C, Cao A, Moi P.
    Prenat Diagn; 2006 May; 26(5):418-9. PubMed ID: 16532523
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):130-134. PubMed ID: 32039781
    [Abstract] [Full Text] [Related]

  • 10. 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; 23(7):564-5. PubMed ID: 12868084
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis and fetopathological findings in a fetus with ring chromosome 18.
    Thies U, Bartels I, von Beust G, Bink K, Hansmann I, Rehder H, Suren A, Zoll B.
    Fetal Diagn Ther; 1998 Jul; 13(5):315-20. PubMed ID: 9813427
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W.
    Gene; 2013 Oct 15; 529(1):163-8. PubMed ID: 23933417
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 24(1):38-44. PubMed ID: 14755408
    [Abstract] [Full Text] [Related]

  • 14. Molecular-cytogenetic investigations of ten term placentae in cases of prenatally diagnosed mosaicism.
    Schubert R, Raff R, Schwanitz G.
    Prenat Diagn; 1996 Oct 15; 16(10):907-13. PubMed ID: 8938059
    [Abstract] [Full Text] [Related]

  • 15. The fetal phenotype of the 18p-syndrome. Report of a male fetus at twenty-one weeks.
    Göcke H, Muradow I, Stein W.
    Ann Genet; 1988 Oct 15; 31(1):60-4. PubMed ID: 3281573
    [Abstract] [Full Text] [Related]

  • 16. Complete discrepancy between abnormal fetal karyotypes predicted by QF-PCR rapid testing and karyotyped cultured cells in a first-trimester CVS.
    Waters JJ, Walsh S, Levett LJ, Liddle S, Akinfenwa Y.
    Prenat Diagn; 2006 Oct 15; 26(10):892-7. PubMed ID: 16906600
    [Abstract] [Full Text] [Related]

  • 17. Fetoplacental chromosomal discrepancy.
    Farra C, Giudicelli B, Pellissier MC, Philip N, Piquet C.
    Prenat Diagn; 2000 Mar 15; 20(3):190-3. PubMed ID: 10719319
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of monosomy 18 and ring chromosome 18 mosaicism.
    Eiben B, Unger M, Stoltenberg G, Rutt G, Goebel R, Meyer A, Gamerdinger U, Hammans W, Hansen S, Hauss H.
    Prenat Diagn; 1992 Nov 15; 12(11):945-50. PubMed ID: 1494547
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villi.
    Anselem O, Bazin A, Mechler C, Blin G, Garel C, Aboura A, Moutard ML, Mandelbrot L.
    Fetal Diagn Ther; 2010 Nov 15; 28(3):180-5. PubMed ID: 20829580
    [Abstract] [Full Text] [Related]

  • 20. Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3.
    Chen CP, Lin YH, Chou SY, Su YN, Chern SR, Chen YT, Town DD, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2012 Mar 15; 51(1):71-6. PubMed ID: 22482972
    [Abstract] [Full Text] [Related]

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