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Journal Abstract Search

88 related items for PubMed ID: 7541608

  • 21. [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
    [Abstract] [Full Text] [Related]

  • 22. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
    Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, Okada A, Ohishi S, Nabetani A, Morisaki H, Nakayama M, Niikawa N, Mukai T.
    Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187
    [Abstract] [Full Text] [Related]

  • 23. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
    Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, Grundy R, Bowdin SC, Riccio A, Sebastio G, Bliek J, Schofield PN, Reik W, Macdonald F, Maher ER.
    Eur J Hum Genet; 2005 Sep; 13(9):1025-32. PubMed ID: 15999116
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  • 24. [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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  • 25. Beckwith Wiedemann syndrome: presentation of a case report.
    Narea Matamala G, Fernández Toro Mde L, Villalabeitía Ugarte E, Landaeta Mendoza M.
    Med Oral Patol Oral Cir Bucal; 2008 Oct 01; 13(10):E640-3. PubMed ID: 18830172
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  • 26.
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  • 27. Intrauterine growth and ultrasound findings in fetuses with Beckwith-Wiedemann syndrome.
    Ranzini AC, Day-Salvatore D, Turner T, Smulian JC, Vintzileos AM.
    Obstet Gynecol; 1997 Apr 01; 89(4):538-42. PubMed ID: 9083309
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  • 28. Are children born after assisted reproductive technology at increased risk for adverse health outcomes?
    Schieve LA, Rasmussen SA, Buck GM, Schendel DE, Reynolds MA, Wright VC.
    Obstet Gynecol; 2004 Jun 01; 103(6):1154-63. PubMed ID: 15172847
    [Abstract] [Full Text] [Related]

  • 29. Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome.
    Chitayat D, Rothchild A, Ling E, Friedman JM, Couch RM, Yong SL, Baldwin VJ, Hall JG.
    Am J Med Genet; 1990 Aug 01; 36(4):434-9. PubMed ID: 2389800
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  • 30. Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature.
    Pettenati MJ, Haines JL, Higgins RR, Wappner RS, Palmer CG, Weaver DD.
    Hum Genet; 1986 Oct 01; 74(2):143-54. PubMed ID: 3770742
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  • 31. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
    Enklaar T, Zabel BU, Prawitt D.
    Expert Rev Mol Med; 2006 Jul 17; 8(17):1-19. PubMed ID: 16842655
    [Abstract] [Full Text] [Related]

  • 32. Analysis of CDKN1C in Beckwith Wiedemann syndrome.
    Algar E, Brickell S, Deeble G, Amor D, Smith P.
    Hum Mutat; 2000 Jul 17; 15(6):497-508. PubMed ID: 10862080
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  • 34. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
    Kubota T, Saitoh S, Matsumoto T, Narahara K, Fukushima Y, Jinno Y, Niikawa N.
    Am J Med Genet; 1994 Feb 15; 49(4):378-83. PubMed ID: 7909196
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  • 36. 47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome.
    Fryns JP, Kleczkowska A, Van den Berghe H.
    Ann Genet; 1986 Feb 15; 29(2):112-3. PubMed ID: 3490205
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  • 37.
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  • 38. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
    Eggermann T.
    Horm Res; 2009 Apr 15; 71 Suppl 2():30-5. PubMed ID: 19407494
    [Abstract] [Full Text] [Related]

  • 39. Fetal and neonatal hepatic tumors.
    Isaacs H.
    J Pediatr Surg; 2007 Nov 15; 42(11):1797-803. PubMed ID: 18022426
    [Abstract] [Full Text] [Related]

  • 40. A child with Beckwith-Wiedemann syndrome and posterior urethral valves.
    Buyukcelik M, Satar N, Dursun H, Bayazit Y, Bayazit AK, Soran M, Noyan A, Anarat A.
    Genet Couns; 2005 Nov 15; 16(1):41-4. PubMed ID: 15844777
    [Abstract] [Full Text] [Related]

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