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Journal Abstract Search

158 related items for PubMed ID: 6854451

  • 1. Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome.
    Waziri M, Patil SR, Hanson JW, Bartley JA.
    J Pediatr; 1983 Jun; 102(6):873-6. PubMed ID: 6854451
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  • 2. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
    Fryns JP, Kleczkowska A, Devriendt K, Devliegher H, Van den Berghe H.
    Genet Couns; 1993 Jun; 4(1):37-41. PubMed ID: 8471219
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  • 3. Beckwith-Wiedemann syndrome.
    Norman AM, Read AP, Donnai D.
    J Med Genet; 1992 Sep; 29(9):679. PubMed ID: 1404305
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  • 6. Deletion of chromosome 11(p11p13) in a patient with Beckwith-Wiedemann syndrome.
    Schmutz SM.
    Clin Genet; 1986 Sep; 30(3):154-6. PubMed ID: 3780031
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  • 7. 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 Sep; 48(2):159-66. PubMed ID: 16053907
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  • 8. Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndrome.
    Bischoff FZ, Feldman GL, McCaskill C, Subramanian S, Hughes MR, Shaffer LG.
    Hum Mol Genet; 1995 Mar; 4(3):395-9. PubMed ID: 7795593
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  • 9. 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 Mar; 28(2):97-101. PubMed ID: 3876070
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  • 10. 47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome.
    Fryns JP, Kleczkowska A, Van den Berghe H.
    Ann Genet; 1986 Mar; 29(2):112-3. PubMed ID: 3490205
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  • 11. 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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  • 12. Beckwith-Wiedemann syndrome, tumourigenesis and imprinting.
    Junien C.
    Curr Opin Genet Dev; 1992 Jun; 2(3):431-8. PubMed ID: 1504618
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  • 15. Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy.
    Turleau C, de Grouchy J.
    Ann Genet; 1985 Jun; 28(2):93-6. PubMed ID: 2994545
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  • 17. Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11.
    Nyström A, Cheetham JE, Engström W, Schofield PN.
    Eur J Pediatr; 1992 Jul; 151(7):511-4. PubMed ID: 1356785
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