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Journal Abstract Search

87 related items for PubMed ID: 2764022

  • 1. 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; 33(2):155-60. PubMed ID: 2764022
    [Abstract] [Full Text] [Related]

  • 2. The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity.
    Niikawa N, Ishikiriyama S, Takahashi S, Inagawa A, Tonoki H, Ohta Y, Hase N, Kamei T, Kajii T.
    Am J Med Genet; 1986 May; 24(1):41-55. PubMed ID: 3706412
    [Abstract] [Full Text] [Related]

  • 3. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family.
    Best LG, Hoekstra RE.
    Am J Med Genet; 1981 May; 9(4):291-9. PubMed ID: 7294068
    [Abstract] [Full Text] [Related]

  • 4. Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.
    Barr CL, Best L, Weksberg R.
    Am J Med Genet; 2001 Nov 22; 104(2):120-6. PubMed ID: 11746041
    [Abstract] [Full Text] [Related]

  • 5. Monozygotic twinning and Wiedemann-Beckwith syndrome.
    Clayton-Smith J, Read AP, Donnai D.
    Am J Med Genet; 1992 Feb 15; 42(4):633-7. PubMed ID: 1609846
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Familial posterior helical ear pits and Wiedemann-Beckwith syndrome.
    Best LG.
    Am J Med Genet; 1991 Aug 01; 40(2):188-95. PubMed ID: 1897573
    [Abstract] [Full Text] [Related]

  • 8. Wiedemann-Beckwith syndrome in apparently discordant monozygotic twins.
    Olney AH, Buehler BA, Waziri M.
    Am J Med Genet; 1988 Mar 01; 29(3):491-9. PubMed ID: 3376993
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 38(1):52-7. PubMed ID: 2012133
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism.
    Martínez y Martínez R, Ocampo-Campos R, Pérez-Arroyo R, Corona-Rivera E, Cantú JM.
    Eur J Pediatr; 1985 Jan 15; 143(3):233-5. PubMed ID: 3987723
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 74(2):143-54. PubMed ID: 3770742
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. 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 08; 14(2):171-3. PubMed ID: 8841187
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M, Pelosse B, Laroche L, Vazquez MP.
    J Fr Ophtalmol; 2001 May 15; 24(5):479-81. PubMed ID: 11397983
    [Abstract] [Full Text] [Related]

  • 18. Familial recurrent intrahepatic cholestasis of pregnancy: a genetic study providing evidence for transmission of a sex-limited, dominant trait.
    Holzbach RT, Sivak DA, Braun WE.
    Gastroenterology; 1983 Jul 15; 85(1):175-9. PubMed ID: 6852450
    [Abstract] [Full Text] [Related]

  • 19. 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]

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