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Journal Abstract Search

293 related items for PubMed ID: 8953635

  • 21. Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases.
    Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, Howard-Peebles PN, Wilson RD.
    Am J Med Genet; 1996 Nov 11; 65(4):348-52. PubMed ID: 8923948
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  • 22. Prenatal diagnosis of the distal 11q deletion and review of the literature.
    Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Chen LF, Wang W.
    Prenat Diagn; 2004 Feb 11; 24(2):130-6. PubMed ID: 14974122
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  • 23. 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 11; 23(7):564-5. PubMed ID: 12868084
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  • 24. Transposition of great arteries in an infant born after prenatal diagnosis of trisomy 20 mosaicism.
    Karaoguz MY, Pala E, Kula S, Karaer K, Kan D, Nas T, Tunaoglu S.
    Genet Couns; 2007 Jul 11; 18(4):437-43. PubMed ID: 18286825
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  • 25. 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 Jul 11; 53(4):197-200. PubMed ID: 20350623
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  • 26. 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 11; 24(2):137-43. PubMed ID: 14974123
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  • 27. Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.
    Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK.
    Prenat Diagn; 2002 Dec 11; 22(12):1076-85. PubMed ID: 12454962
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  • 28. Maternal uniparental disomy 16 and genetic counseling: new case and survey of published cases.
    Eggermann T, Curtis M, Zerres K, Hughes HE.
    Genet Couns; 2004 Dec 11; 15(2):183-90. PubMed ID: 15287418
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  • 29. Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling.
    Berghella V, Wapner RJ, Yang-Feng T, Mahoney MJ.
    Prenat Diagn; 1998 Apr 11; 18(4):384-9. PubMed ID: 9602487
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  • 30. 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 11; 26(9):778-81. PubMed ID: 16810710
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  • 31. Sonographically detected fetal and placental abnormalities associated with trisomy 16 confined to the placenta. A case report and review of the literature.
    Astner A, Schwinger E, Caliebe A, Jonat W, Gembruch U.
    Prenat Diagn; 1998 Dec 11; 18(12):1308-15. PubMed ID: 9885025
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  • 33. [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 Dec 11; 24(6):606-9. PubMed ID: 8830080
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  • 34. Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
    Wallerstein R, Yu MT, Neu RL, Benn P, Lee Bowen C, Crandall B, Disteche C, Donahue R, Harrison B, Hershey D, Higgins RR, Jenkins LS, Jackson-Cook C, Keitges E, Khodr G, Lin CC, Luthardt FW, Meisner L, Mengden G, Patil SR, Rodriguez M, Sciorra LJ, Shaffer LG, Stetten G, Van Dyke DL, Wang H.
    Prenat Diagn; 2000 Feb 11; 20(2):103-22. PubMed ID: 10694683
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  • 35. Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature.
    Redaelli S, Sala E, Roncaglia N, Colombo C, Crosti F, Villa N, Tagliabue P, Cappellini A, Dalprà L.
    Prenat Diagn; 2005 Feb 11; 25(2):140-7. PubMed ID: 15712378
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  • 39. Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15.
    Slater HR, Vaux C, Pertile M, Burgess T, Petrovic V.
    Prenat Diagn; 1997 Feb 11; 17(2):109-13. PubMed ID: 9061757
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  • 40. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
    Chen CP, Su YN, Chern SR, Chen YT, Wu PS, Su JW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2012 Dec 11; 51(4):603-11. PubMed ID: 23276565
    [Abstract] [Full Text] [Related]

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