1. Complexe malformatif familial avec hernie ombilicale et macroglossie. Un 'syndrome nouveau'?;lWiedemann HR;J Genet Hum,1964
2. The Beckwith-Wiedemann syndrome;Fillipi, G.; McKusick, V.A.;Medicine,1970
3. Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling;Berry, C.A.; Belton, E.M.; Chantler, C.;J Med Genet,1980
4. Localization of insulin like growth factor genes to human chromosome 11 and 12;Tricoli, J.V.; Rall, L.B.; Scott, J.; Bell, G.I.; Shows, T.B.;Nature,1984
5. Abnormality of chromosome 11 in patients with features of BeckwithWeidemann syndrome;Waziri, M.; Patil, SR, Hanson; JW, Bartley; J.A.;J Pediatr,1983