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Journal Abstract Search

184 related items for PubMed ID: 8533839

  • 21. Mosaic vs. nonmosaic trisomy 9: report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature.
    Cantú ES, Eicher DJ, Pai GS, Donahue CJ, Harley RA.
    Am J Med Genet; 1996 Apr 24; 62(4):330-5. PubMed ID: 8723059
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  • 22. GATA1 mutation and trisomy 21 are required only in haematopoietic cells for development of transient myeloproliferative disorder.
    Carpenter E, Valverde-Garduno V, Sternberg A, Mitchell C, Roberts I, Vyas P, Vora A.
    Br J Haematol; 2005 Feb 24; 128(4):548-51. PubMed ID: 15686466
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  • 23. Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases.
    Seghezzi L, Maserati E, Minelli A, Dellavecchia C, Addis P, Locatelli F, Angioni A, Balloni P, Miano C, Cavalli P, Danesino C, Pasquali F.
    Genes Chromosomes Cancer; 1996 Oct 24; 17(2):94-101. PubMed ID: 8913726
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  • 24. [Diminished in vitro colony forming capacity of bone marrow cells in a case of chromosome 8 trisomy (mosaicism): criteria for "high risk" pre-leukemia syndrome].
    Cornaglia-Ferraris P, Ghio R, Barabino A, Perlino GF, Maggio A, Parodi MT, Massimo L.
    Boll Ist Sieroter Milan; 1981 Oct 24; 60(1):69-73. PubMed ID: 7272014
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  • 27. Interstitial deletion of chromosome 5, del(5q), in a newborn with Down syndrome and an unusual hematologic disorder.
    Adams RH, Lemons RS, Thangavelu M, Le Beau MM, Christensen RD.
    Am J Hematol; 1989 Aug 24; 31(4):273-9. PubMed ID: 2525873
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  • 32. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA, Schwartz S, Black CJ, Jaswaney V.
    Am J Med Genet; 1997 Sep 05; 71(4):406-13. PubMed ID: 9286446
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  • 33. [Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].
    Ronger S, Till M, Kanitakis J, Balme B, Thomas L.
    Ann Dermatol Venereol; 2003 Nov 05; 130(11):1033-8. PubMed ID: 14724538
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  • 38. Congenital leukaemia in Down Syndrome--a case report.
    Aier M, Zadeng T, Basu D, Biswal N, Nalini P.
    Indian J Pathol Microbiol; 2002 Jul 05; 45(3):355-7. PubMed ID: 12785186
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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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