94 related articles for article (PubMed ID: 8488888)
1. Monozygotic twinning and Wiedemann-Beckwith syndrome.
Franceschini P; Guala A; Vardeu MP; Franceschini D
Am J Med Genet; 1993 May; 46(3):353-4. PubMed ID: 8488888
[No Abstract] [Full Text] [Related]
2. Monozygotic twinning and Wiedemann-Beckwith syndrome.
Clayton-Smith J; Read AP; Donnai D
Am J Med Genet; 1992 Feb; 42(4):633-7. PubMed ID: 1609846
[TBL] [Abstract][Full Text] [Related]
3. 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; 30(3):821-33. PubMed ID: 3189402
[TBL] [Abstract][Full Text] [Related]
4. Wiedemann-Beckwith syndrome in apparently discordant monozygotic twins.
Olney AH; Buehler BA; Waziri M
Am J Med Genet; 1988 Mar; 29(3):491-9. PubMed ID: 3376993
[TBL] [Abstract][Full Text] [Related]
5. Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome.
Orstavik RE; Tommerup N; Eiklid K; Orstavik KH
Am J Med Genet; 1995 Mar; 56(2):210-4. PubMed ID: 7625447
[TBL] [Abstract][Full Text] [Related]
6. Wiedemann-Beckwith syndrome in one of monozygotic twins.
Bose B; Wilkie RA; Madlom M; Forsyth JS; Faed MJ
Arch Dis Child; 1985 Dec; 60(12):1191-2. PubMed ID: 4091589
[TBL] [Abstract][Full Text] [Related]
7. 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; 61(3):253-7. PubMed ID: 8741870
[TBL] [Abstract][Full Text] [Related]
8. [Wiedemann-Beckwith syndrome].
Kunze J; Wiedemann HR
Ergeb Inn Med Kinderheilkd; 1993; 61():303-38. PubMed ID: 8223387
[No Abstract] [Full Text] [Related]
9. Diagnosis and management of the phenotypic spectrum of twins with Beckwith-Wiedemann syndrome.
Cohen JL; Duffy KA; Sajorda BJ; Hathaway ER; Gonzalez-Gandolfi CX; Richards-Yutz J; Gunter AT; Ganguly A; Kaplan J; Deardorff MA; Kalish JM
Am J Med Genet A; 2019 Jul; 179(7):1139-1147. PubMed ID: 31067005
[TBL] [Abstract][Full Text] [Related]
10. Monozygotic twins discordant for vascular malformations and dysregulated growth.
Oduber CE; Bliek J; van der Horst CM; van Steensel MA; Hennekam RC
Eur J Med Genet; 2010; 53(1):14-8. PubMed ID: 19716450
[TBL] [Abstract][Full Text] [Related]
11. Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.
Sun F; Hara S; Tomita C; Tanoue Y; Yatsuki H; Higashimoto K; Soejima H
Am J Med Genet A; 2021 Oct; 185(10):3062-3067. PubMed ID: 34037318
[TBL] [Abstract][Full Text] [Related]
12. Beckwith-Wiedemann syndrome.
Weksberg R; Shuman C; Smith AC
Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
[TBL] [Abstract][Full Text] [Related]
13. Index of suspicion. Case 2. Wiedemann-Beckwith syndrome.
Stratakis CA
Pediatr Rev; 1995 Nov; 16(11):433, 434-5. PubMed ID: 8539195
[No Abstract] [Full Text] [Related]
14. Wiedemann-Beckwith syndrome in one of monozygotic twins.
Brown S
Arch Dis Child; 1986 Jul; 61(7):717. PubMed ID: 3740918
[No Abstract] [Full Text] [Related]
15. [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
[TBL] [Abstract][Full Text] [Related]
16. Wiedemann-Beckwith syndrome with congenital central hypothyroidism in one of monozygotic twins.
Chien CH; Lee JS; Tsai WY; Wang TR
J Formos Med Assoc; 1990 Feb; 89(2):132-6. PubMed ID: 1973721
[TBL] [Abstract][Full Text] [Related]
17. [Beckwith-Wiedemann syndrome in 3 sisters].
Almazán C; Jullian M; Aranda W
Rev Chil Pediatr; 1984; 55(5):340-3. PubMed ID: 6535198
[No Abstract] [Full Text] [Related]
18. 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; 16(1):41-4. PubMed ID: 15844777
[TBL] [Abstract][Full Text] [Related]
19. Imprinting errors and developmental asymmetry.
Bestor TH
Philos Trans R Soc Lond B Biol Sci; 2003 Aug; 358(1436):1411-5. PubMed ID: 14511489
[TBL] [Abstract][Full Text] [Related]
20. [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; 91(11):837-40. PubMed ID: 16264244
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
