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255 related items for PubMed ID: 8834049

  • 1. Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review.
    Markovic VD, Chitayat DA, Ritchie SM, Chodakowski BA, Hutton EM.
    Am J Med Genet; 1996 Feb 02; 61(4):363-70. PubMed ID: 8834049
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  • 2. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
    Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH.
    Prenat Diagn; 1996 Apr 02; 16(4):323-32. PubMed ID: 8734806
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  • 3. 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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  • 4. 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 11; 73(8):577-82. PubMed ID: 16007591
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  • 5. Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC).
    Prenat Diagn; 1999 Jan 11; 19(1):29-35. PubMed ID: 10073903
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  • 6. Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.
    Grati FR, Grimi B, Frascoli G, Di Meco AM, Liuti R, Milani S, Trotta A, Dulcetti F, Grosso E, Miozzo M, Maggi F, Simoni G.
    Eur J Hum Genet; 2006 Mar 11; 14(3):282-8. PubMed ID: 16418738
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  • 7. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus.
    Schlegel M, Baumer A, Riegel M, Wiedemann U, Schinzel A.
    Prenat Diagn; 2002 May 11; 22(5):418-21. PubMed ID: 12001199
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  • 8. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK, Hardin EL, Pacheco C, Kuslich CD, Donlon TA.
    Obstet Gynecol; 1996 May 11; 87(5 Pt 2):856-60. PubMed ID: 8677115
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  • 9. 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 May 11; 53(4):197-200. PubMed ID: 20350623
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  • 10. 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 May 11; 7(4):421-6. PubMed ID: 10352932
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  • 18. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization.
    Wolstenholme J.
    Prenat Diagn; 1996 Jun 11; 16(6):511-24. PubMed ID: 8809892
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  • 19. A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9.
    Wilkinson TA, James RS, Crolla JA, Cockwell AE, Campbell PL, Temple IK.
    Prenat Diagn; 1996 Apr 11; 16(4):371-4. PubMed ID: 8734817
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