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113 related items for PubMed ID: 2309794

  • 1. Neuroblastoma in a child with Wiedemann-Beckwith syndrome.
    Chitayat D, Friedman JM, Dimmick JE.
    Am J Med Genet; 1990 Mar; 35(3):433-6. PubMed ID: 2309794
    [Abstract] [Full Text] [Related]

  • 2. Congenital gastric teratoma in Wiedemann-Beckwith syndrome.
    Falik-Borenstein TC, Korenberg JR, Davos I, Platt LD, Gans S, Goodman B, Schreck R, Graham JM.
    Am J Med Genet; 1991 Jan; 38(1):52-7. PubMed ID: 2012133
    [Abstract] [Full Text] [Related]

  • 3. Two pairs of male monozygotic twins discordant for Wiedemann-Beckwith syndrome.
    Leonard NJ, Bernier FP, Rudd N, Machin GA, Bamforth F, Bamforth S, Grundy P, Johnson C.
    Am J Med Genet; 1996 Jan 22; 61(3):253-7. PubMed ID: 8741870
    [Abstract] [Full Text] [Related]

  • 4. Molecular genetics of Wiedemann-Beckwith syndrome.
    Li M, Squire JA, Weksberg R.
    Am J Med Genet; 1998 Oct 02; 79(4):253-9. PubMed ID: 9781904
    [Abstract] [Full Text] [Related]

  • 5. Unusual evolution of Wilms tumor in a patient with Wiedemann-Beckwith syndrome.
    Rey C, del Molino A, Santos F, Malaga S, Crespo M.
    Helv Paediatr Acta; 1988 Aug 02; 43(1-2):91-6. PubMed ID: 2844706
    [Abstract] [Full Text] [Related]

  • 6. [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 02; 91(11):837-40. PubMed ID: 16264244
    [Abstract] [Full Text] [Related]

  • 7. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M, Pelosse B, Laroche L, Vazquez MP.
    J Fr Ophtalmol; 2001 May 02; 24(5):479-81. PubMed ID: 11397983
    [Abstract] [Full Text] [Related]

  • 8. Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome.
    Litz CE, Taylor KA, Qiu JS, Pescovitz OH, de Martinville B.
    Am J Med Genet; 1988 Jul 02; 30(3):821-33. PubMed ID: 3189402
    [Abstract] [Full Text] [Related]

  • 9. Heterogeneity in Wiedemann-Beckwith syndrome: anthropometric evidence.
    Moore ES, Ward RE, Escobar LF, Carlin ME.
    Am J Med Genet; 2000 Feb 14; 90(4):283-90. PubMed ID: 10710224
    [Abstract] [Full Text] [Related]

  • 10. Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy.
    Turleau C, de Grouchy J.
    Ann Genet; 1985 Feb 14; 28(2):93-6. PubMed ID: 2994545
    [Abstract] [Full Text] [Related]

  • 11. Incidence of abdominal tumors in syndromic and idiopathic hemihypertrophy/isolated hemihyperplasia.
    Dempsey-Robertson M, Wilkes D, Stall A, Bush P.
    J Pediatr Orthop; 2012 Feb 14; 32(3):322-6. PubMed ID: 22411341
    [Abstract] [Full Text] [Related]

  • 12. 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 Feb 14; 16(1):41-4. PubMed ID: 15844777
    [Abstract] [Full Text] [Related]

  • 13. Longitudinal observations on 15 children with Wiedemann-Beckwith syndrome.
    Weng EY, Moeschler JB, Graham JM.
    Am J Med Genet; 1995 May 08; 56(4):366-73. PubMed ID: 7541608
    [Abstract] [Full Text] [Related]

  • 14. Nonimmune fetal hydrops and placentomegaly: diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH.
    Drut RM, Drut R.
    Am J Med Genet; 1996 Mar 15; 62(2):145-9. PubMed ID: 8882394
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Miscellaneous genodermatoses: Beckwith-Wiedemann syndrome, Birt-Hogg-Dube syndrome, familial atypical multiple mole melanoma syndrome, hereditary tylosis, incontinentia pigmenti, and supernumerary nipples.
    Cohen PR, Kurzrock R.
    Dermatol Clin; 1995 Jan 15; 13(1):211-29. PubMed ID: 7712645
    [Abstract] [Full Text] [Related]

  • 17. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.
    Weksberg R, Shen DR, Fei YL, Song QL, Squire J.
    Nat Genet; 1993 Oct 15; 5(2):143-50. PubMed ID: 8252039
    [Abstract] [Full Text] [Related]

  • 18. Dominant inheritance of Wiedemann-Beckwith syndrome: further evidence for transmission of "unstable premutation" through carrier women.
    Aleck KA, Hadro TA.
    Am J Med Genet; 1989 Jun 15; 33(2):155-60. PubMed ID: 2764022
    [Abstract] [Full Text] [Related]

  • 19. [Malignancy risk and Wiedemann-Beckwith syndrome: what follow-up to provide?].
    Santiago J, Muszlak M, Samson C, Goulois E, Glorion A, Atale A, Ranaivoarivony V, Hebert JC, Bouvier R, Cordier MP.
    Arch Pediatr; 2008 Sep 15; 15(9):1498-502. PubMed ID: 18674889
    [Abstract] [Full Text] [Related]

  • 20. Hypercalciuria in Beckwith-Wiedemann syndrome.
    Goldman M, Shuman C, Weksberg R, Rosenblum ND.
    J Pediatr; 2003 Feb 15; 142(2):206-8. PubMed ID: 12584548
    [Abstract] [Full Text] [Related]

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