Abstract
A pair of monozygotic twins discordant for Wiedemann-Beckwith syndrome is described. The probability of monozygosity is 0.995. This observation suggests that the syndrome is unlikely to be under single gene control and genetic counselling should be based on multifactorial inheritance.
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Selected References
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- Berry A. C., Belton E. M., Chantler C. Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling. J Med Genet. 1980 Apr;17(2):136–138. doi: 10.1136/jmg.17.2.136. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Filippi G., Mckusick V. A. The Beckwith-Wiedmann syndrome. Medicine (Baltimore) 1970 Jul;49(4):279–298. doi: 10.1097/00005792-197007000-00002. [DOI] [PubMed] [Google Scholar]
- Schinzel A. A., Smith D. W., Miller J. R. Monozygotic twinning and structural defects. J Pediatr. 1979 Dec;95(6):921–930. doi: 10.1016/s0022-3476(79)80278-4. [DOI] [PubMed] [Google Scholar]
- Tricoli J. V., Rall L. B., Scott J., Bell G. I., Shows T. B. Localization of insulin-like growth factor genes to human chromosomes 11 and 12. 1984 Aug 30-Sep 5Nature. 310(5980):784–786. doi: 10.1038/310784a0. [DOI] [PubMed] [Google Scholar]
- WIEDEMANN H. R. COMPLEXE MALFORMATIF FAMILIAL AVEC HERNIE OMBILICALE ET MACROGLOSSIE--UN "SYNDROME NOUVEAU"? J Genet Hum. 1964 Sep;13:223–232. [PubMed] [Google Scholar]
- Waziri M., Patil S. R., Hanson J. W., Bartley J. A. Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr. 1983 Jun;102(6):873–876. doi: 10.1016/s0022-3476(83)80014-6. [DOI] [PubMed] [Google Scholar]
