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277 related items for PubMed ID: 3876070

  • 1. Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases.
    Journel H, Lucas J, Allaire C, Le Mée F, Defawe G, Lecornu M, Jouan H, Roussey M, Le Marec B.
    Ann Genet; 1985; 28(2):97-101. PubMed ID: 3876070
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  • 2. Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.
    Turleau C, de Grouchy J, Chavin-Colin F, Martelli H, Voyer M, Charlas R.
    Hum Genet; 1984; 67(2):219-21. PubMed ID: 6745943
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  • 3. Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy.
    Turleau C, de Grouchy J.
    Ann Genet; 1985; 28(2):93-6. PubMed ID: 2994545
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  • 4. 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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  • 5. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M, Pelosse B, Laroche L, Vazquez MP.
    J Fr Ophtalmol; 2001 May; 24(5):479-81. PubMed ID: 11397983
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  • 9. 47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome.
    Fryns JP, Kleczkowska A, Van den Berghe H.
    Ann Genet; 1986 May; 29(2):112-3. PubMed ID: 3490205
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  • 10. [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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  • 11. [Wiedemann-Beckwith syndrome: clinical and epidemiological analysis of a consecutive series of cases in Spain].
    Arroyo Carrera I, Martínez-Frías ML, Egüés Jimeno J, García Martínez MJ, Eloína Cimadevilla Sánchez C, Bermejo Sánchez E.
    An Esp Pediatr; 1999 Feb; 50(2):161-5. PubMed ID: 10199027
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  • 12. A new case of Beckwith-Wiedemann syndrome with an 11p15 duplication of paternal origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat].
    Krajewska-Walasek M, Gutkowska A, Mospinek-Krasnopolska M, Chrzanowska K.
    Acta Genet Med Gemellol (Roma); 1996 Feb; 45(1-2):245-50. PubMed ID: 8872040
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  • 14. 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; 56(10):546-50. PubMed ID: 23892181
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  • 15. Jacobsen and Beckwith-Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy.
    Putoux A, Labalme A, André JM, Till M, Schluth-Bolard C, Berard J, Bertrand Y, Edery P, Putet G, Sanlaville D.
    Am J Med Genet A; 2013 Feb; 161A(2):331-7. PubMed ID: 23322614
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  • 16. [Beckwith-Wiedemann syndrome: study of eleven cases].
    Solsona-Narbón B, Castillo Laita JA, Buñuel Alvarez JC, Elías Pollina J, Loris Pablo C, Romo Montejo A, Esteban Ibarz J, Bello Andrés E.
    An Esp Pediatr; 1992 Mar; 36(3):181-5. PubMed ID: 1580425
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  • 17. Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives.
    Cohen MM.
    Pediatr Dev Pathol; 2005 Mar; 8(3):287-304. PubMed ID: 16010495
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  • 18. 11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency.
    Jurkiewicz D, Kugaudo M, Tańska A, Wawrzkiewicz-Witkowska A, Tomaszewska A, Kucharczyk M, Cieślikowska A, Ciara E, Krajewska-Walasek M.
    Pediatr Int; 2015 Jun; 57(3):486-91. PubMed ID: 26012727
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  • 19. Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
    South ST, Whitby H, Maxwell T, Aston E, Brothman AR, Carey JC.
    Am J Med Genet A; 2008 Oct 15; 146A(20):2691-7. PubMed ID: 18798325
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  • 20. 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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