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Journal Abstract Search

237 related items for PubMed ID: 9401109

  • 21. 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; 16(6):511-24. PubMed ID: 8809892
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  • 22. Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.
    Flori E, Girodon E, Samama B, Becmeur F, Viville B, Girard-Lemaire F, Doray B, Schluth C, Marcellin L, Boehm N, Goossens M, Pingault V.
    Eur J Hum Genet; 2005 Sep; 13(9):1013-8. PubMed ID: 15915162
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  • 23. Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case.
    Martínez A, Ramos S, González-del Angel A, Alcántara MA, Molina B, Carnevale A.
    Rev Invest Clin; 2007 Sep; 59(6):444-8. PubMed ID: 18402336
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  • 24. Trisomy 9 mosaicism syndrome. A case report and review of the literature.
    Tarani L, Colloridi F, Raguso G, Rizzuti A, Bruni L, Tozzi MC, Palermo D, Panero A, Vignetti P.
    Ann Genet; 1994 Sep; 37(1):14-20. PubMed ID: 8010707
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  • 25. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM.
    Genet Couns; 2007 Sep; 18(1):29-48. PubMed ID: 17515299
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  • 26. Management of prenatally detected trisomy 8 mosaicism.
    van Haelst MM, Van Opstal D, Lindhout D, Los FJ.
    Prenat Diagn; 2001 Dec; 21(12):1075-8. PubMed ID: 11746167
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  • 27. Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS.
    Allen SK, Luharia A, Gould CP, MacDonald F, Larkins S, Davison EV.
    Prenat Diagn; 2006 Dec; 26(12):1160-7. PubMed ID: 17063531
    [Abstract] [Full Text] [Related]

  • 28. 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; 46(2):115-7. PubMed ID: 16732770
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  • 32. A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism.
    Von Beust G, Bartels I, Zoll B.
    Genet Couns; 2003 Jun; 14(1):67-74. PubMed ID: 12725591
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  • 33. [Trisomy 22--prenatal findings in various developmental stages].
    Zerres K, Niesen M, Schwanitz G, Hansmann M.
    Geburtshilfe Frauenheilkd; 1988 Oct; 48(10):720-3. PubMed ID: 3234704
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  • 34. A search on karyotypic mosaicism in mongoloid patients and their parents.
    Kasahara S, Viegas-Pequignot EM, Frota-Pessoa O.
    Rev Bras Pesqui Med Biol; 1977 Aug; 10(4):225-35. PubMed ID: 143677
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  • 35. Trisomy 8 mosaicism: a further five cases illustrating marked clinical and cytogenetic variability.
    Jordan MA, Marques I, Rosendorff J, de Ravel TJ.
    Genet Couns; 1998 Aug; 9(2):139-46. PubMed ID: 9664211
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  • 40. Patient with trisomy 6 mosaicism.
    Miller KR, Mühlhaus K, Herbst RA, Bohnhorst B, Böhmer S, Arslan-Kirchner M.
    Am J Med Genet; 2001 Apr 22; 100(2):103-5. PubMed ID: 11298369
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