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PUBMED FOR HANDHELDS

Journal Abstract Search


280 related items for PubMed ID: 8471219

  • 1. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
    Fryns JP, Kleczkowska A, Devriendt K, Devliegher H, Van den Berghe H.
    Genet Couns; 1993; 4(1):37-41. PubMed ID: 8471219
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  • 2. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A, Lapunzina P, Palomares M, Molina MA, Galán E, López Pajares I.
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
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  • 3. Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24).
    Gadzicki D, Baumer A, Wey E, Happel CM, Rudolph C, Tönnies H, Neitzel H, Steinemann D, Welte K, Klein C, Schlegelberger B.
    Ann Hum Genet; 2006 Nov; 70(Pt 6):958-64. PubMed ID: 17044870
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  • 5. [Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in Iceland].
    Pálsson GI, Finnsdóttir V, Jóhannsson JH, Ingvarsson S.
    Laeknabladid; 2005 Nov; 91(11):837-40. PubMed ID: 16264244
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  • 7. Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome.
    Negrini M, Sabbioni S, Ohta M, Veronese ML, Rattan S, Junien C, Croce CM.
    Cancer Res; 1995 Jul 01; 55(13):2904-9. PubMed ID: 7796419
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  • 10. Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation.
    Fisher AM, Thomas NS, Cockwell A, Stecko O, Kerr B, Temple IK, Clayton P.
    Hum Genet; 2002 Sep 01; 111(3):290-6. PubMed ID: 12215843
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  • 11. Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
    Duval E, van den Enden A, Vanhaesebrouck P, Speleman F.
    Am J Med Genet; 1994 Aug 15; 52(2):214-7. PubMed ID: 7802011
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  • 13. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P, Kohn G, Litwin A, Nissenkorn I, Katznelson MB, Reisner SH.
    Am J Med Genet; 1989 Jan 15; 32(1):22-6. PubMed ID: 2705479
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  • 15. SNP arrays in Beckwith-Wiedemann syndrome: an improved diagnostic strategy.
    Keren B, Chantot-Bastaraud S, Brioude F, Mach C, Fonteneau E, Azzi S, Depienne C, Brice A, Netchine I, Le Bouc Y, Siffroi JP, Rossignol S.
    Eur J Med Genet; 2013 Oct 15; 56(10):546-50. PubMed ID: 23892181
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  • 16. Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region.
    Russo S, Finelli P, Recalcati MP, Ferraiuolo S, Cogliati F, Dalla Bernardina B, Tibiletti MG, Agosti M, Sala M, Bonati MT, Larizza L.
    J Med Genet; 2006 Aug 15; 43(8):e39. PubMed ID: 16882733
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  • 19. Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5).
    Norman AM, Read AP, Clayton-Smith J, Andrews T, Donnai D.
    Am J Med Genet; 1992 Feb 15; 42(4):638-41. PubMed ID: 1609847
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  • 20. [Wiedemann-Beckwith syndrome: clinical characteristics, constitutional chromosome abnormalities and tumor incidence].
    Haas OA, Zoubek A, Grümayer ER, Ferstl G, Gadner H.
    Klin Padiatr; 1987 Feb 15; 199(4):283-91. PubMed ID: 2821320
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