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Journal Abstract Search

88 related items for PubMed ID: 7541608

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  • 3. [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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  • 4. Follow-up study of patients with Wiedemann-Beckwith syndrome with emphasis on the change in facial appearance over time.
    Hunter AG, Allanson JE.
    Am J Med Genet; 1994 Jun 01; 51(2):102-7. PubMed ID: 8092184
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  • 6. The Beckwith-Wiedemann syndrome: a longitudinal study of the macroglossia and dentofacial complex.
    Friede H, Figueroa AA.
    J Craniofac Genet Dev Biol Suppl; 1985 Jun 01; 1():179-87. PubMed ID: 3877094
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  • 7. 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 01; 33(2):155-60. PubMed ID: 2764022
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  • 8. Recognition and management of the infant with Beckwith-Wiedemann Syndrome.
    Spivey PS, Bradshaw WT.
    Adv Neonatal Care; 2009 Dec 01; 9(6):279-84; quiz 285. PubMed ID: 20010144
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  • 9. Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives.
    Cohen MM.
    Pediatr Dev Pathol; 2005 Dec 01; 8(3):287-304. PubMed ID: 16010495
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  • 11. Neuroblastoma in a child with Wiedemann-Beckwith syndrome.
    Chitayat D, Friedman JM, Dimmick JE.
    Am J Med Genet; 1990 Mar 01; 35(3):433-6. PubMed ID: 2309794
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  • 12. 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
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  • 14. 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
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  • 15. [Beckwith-Wiedemann syndrome: What do you search in prenatal diagnosis? About 14 cases].
    Le Vaillant C, Beneteau C, Chan-Leconte N, David A, Riteau AS.
    Gynecol Obstet Fertil; 2015 Nov 22; 43(11):705-11. PubMed ID: 26542939
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  • 17. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
    Sun FL, Dean WL, Kelsey G, Allen ND, Reik W.
    Nature; 1997 Oct 23; 389(6653):809-15. PubMed ID: 9349812
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  • 18. Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome).
    Kagami M, Kurosawa K, Miyazaki O, Ishino F, Matsuoka K, Ogata T.
    Eur J Hum Genet; 2015 Nov 23; 23(11):1488-98. PubMed ID: 25689926
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  • 20. 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
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