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Journal Abstract Search

379 related items for PubMed ID: 8741873

  • 21. 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; 25(2):140-7. PubMed ID: 15712378
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  • 24. Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC).
    Prenat Diagn; 1999 Jan; 19(1):29-35. PubMed ID: 10073903
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  • 27. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC, Mamunes P, Kou SY, Schmidt J, Mao R, Hsu WT.
    Am J Med Genet; 1998 Dec 04; 80(4):418-22. PubMed ID: 9856575
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  • 28. 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 04; 17(2):109-13. PubMed ID: 9061757
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  • 29. Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20).
    Devriendt K, Matthijs G, Meireleire J, Roelen L, van Buggenhout G, Fryns JP.
    Genet Couns; 1998 Feb 04; 9(4):283-6. PubMed ID: 9894166
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  • 30. Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome.
    Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Chen WL, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2020 Sep 04; 59(5):754-757. PubMed ID: 32917331
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  • 36. 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 04; 16(8):734-40. PubMed ID: 8878284
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  • 37. 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 04; 24(9):693-6. PubMed ID: 15386452
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  • 39. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
    Shashi V, Golden WL, von Kap-Herr C, Wilson WG.
    Am J Med Genet; 1996 Mar 01; 62(1):38-41. PubMed ID: 8779322
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  • 40. Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient.
    Dupont JM, Cuisset L, Cartigny M, Le Tessier D, Vasseur C, Rabineau D, Jeanpierre M.
    Am J Med Genet; 2002 Sep 01; 111(4):405-8. PubMed ID: 12210300
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