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Das Wiedemann-Beckwith-Syndrom: Beobachtung einer oligosymptomatischen Form = Forme incomplète du syndrome de Wiedemann-Beckwith = Incomplete form of Wiedemann-Beckwith syndrome. A case reportLEMKE, J; MEINECKE, P; FRANK, H.-D et al.Monatsschrift für Kinderheilkunde. 1986, Vol 134, Num 8, pp 554-557, issn 0026-9298Article

Anesthetic management in a patient with Beckwith-Wiedemann syndromeFUJITA, A; OKUTANI, R; FUKUDA, T et al.Masui. 1994, Vol 43, Num 9, pp 1389-1391, issn 0021-4892Article

Placentomegaly with massive hydrops of plancental stem Villi, diploid DNA content, and fetal omphaloceles : possible association with Beckwith-Wiedemann syndromeLAGE, J. M.Human pathology. 1991, Vol 22, Num 6, pp 591-597, issn 0046-8177Article

Imprinting and Beckwith-Wiedemann syndromeHOOVERS, J. M. N; DIETRICH, A. J. J; MANNENS, M. M. A. M et al.Lancet (British edition). 1992, Vol 339, Num 8803, issn 0140-6736, p. 1228Article

Mosaic uniparental disomy in Beckwith-Wiedemann syndromeSLATTER, R. E; ELLIOTT, M; WELHAM, K et al.Journal of medical genetics. 1994, Vol 31, Num 10, pp 749-753, issn 0022-2593Article

Inherited microdeletions that give rise to Beckwith-Wiedemann syndromeKANG, M.Clinical genetics. 2005, Vol 67, Num 4, pp 299-300, issn 0009-9163, 2 p.Article

Perlman and Wiedemann-Beckwith syndromes : two distinct conditions associated with Wilms' tumourGRUNDY, R. G; PRITCHARD, J; BARAITSER, M et al.European journal of pediatrics. 1992, Vol 151, Num 12, pp 895-898, issn 0340-6199Conference Paper

Le syndrome de Wiedemann-Beckwith = Beckwith-Wiedemann syndromeHAOUARI, N; STORME, L; GREMILLET, C et al.La Médecine infantile (Paris). 1991, Vol 98, Num 8, pp 631-635, issn 0025-6773Article

Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndromeHIGASHIMOTO, Ken; URANO, Takeshi; MUKAI, Tsunehiro et al.American journal of human genetics. 2003, Vol 73, Num 4, pp 948-956, issn 0002-9297, 9 p.Article

Cleft palate in the Beckwith-Wiedemann syndromeTAKATO, T; KAMEI, M; KATO, K et al.Annals of plastic surgery. 1989, Vol 22, Num 4, pp 347-349, issn 0148-7043Article

Sonographic appearance of placental villous hydrops associted with Beckwith-Wiedemann syndromeHILLSTROM, M. M; BROWN, D. L; WILKINS-HAUG, L et al.Journal of ultrasound in medicine. 1995, Vol 14, Num 1, pp 61-64, issn 0278-4297Article

Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndromeÖRSTAVIK, R. E; TOMMERUP, N; EIKLID, K et al.American journal of medical genetics. 1995, Vol 56, Num 2, pp 210-214, issn 0148-7299Article

Genomic imprinting and cancerBRENTON, J. D; VIVILLE, S; SURANI, M. A et al.Cancer surveys. 1995, Vol 25, pp 161-171, issn 0261-2429Article

Treatment of the cranofacial complications of Beckwith-Wiedemann syndromeMENARD, R. M; DELAIRE, J; SCHENDEL, S. A et al.Plastic and reconstructive surgery (1963). 1995, Vol 96, Num 1, pp 27-33, issn 0032-1052Conference Paper

Genomic imprinting and the Beckwith-Wiedemann syndromeBROWN, K. W; WILLIAMS, J. C; MAITLAND, N. J et al.American journal of human genetics. 1990, Vol 46, Num 5, pp 1000-1001, issn 0002-9297, 2 p.Article

Prenatal ultrasound diagnosis of Beckwith-Wiedemann syndromeSHAH, Y. G; METLAY, L.Journal of clinical ultrasound. 1990, Vol 18, Num 7, pp 597-600, issn 0091-2751Article

Methylation pattern at the KvDMR in a child with Beckwith-Wiedemann syndrome conceived by ICSIGOMES, M. V; COMES, C. C; PINTO, W et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 6, pp 625-629, issn 1552-4825, 5 p.Article

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndromeWEKSBERG, Rosanna; SHUMAN, Cheryl; IVES, Elizabeth et al.Human molecular genetics (Print). 2002, Vol 11, Num 11, pp 1317-1325, issn 0964-6906Article

Low frequency of p57^KIP2 mutation in Beckwith-Wiedemann syndromeLEE, M. P; DEBAUN, M; RANDHAWA, G et al.American journal of human genetics. 1997, Vol 61, Num 2, pp 304-309, issn 0002-9297Article

Macroglossia and ankylossia in Beckwith-Wiedemann syndromePATTERSON, G. T; RAMASASTRY, S. S; DAVIS, J. U et al.Oral surgery, oral medicine, oral pathology. 1988, Vol 65, Num 1, pp 29-31, issn 0030-4220Article

Longitudinal observations on 15 children with Wiedemann-Beckwith syndromeWENG, E. Y; MOESCHLER, J. B; GRAHAM, J. M et al.American journal of medical genetics. 1995, Vol 56, Num 4, pp 366-373, issn 0148-7299Article

Molecular analysis of patients with Wiedemann-Beckwith syndrome. I: Gene dosage on the short arm of chromosome 11NYSTRÖM, A; ENGSTRÖM, W; CHEETHAM, J et al.European journal of pediatrics. 1992, Vol 151, Num 7, pp 504-510, issn 0340-6199Article

Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndromeDIAZ-MEYER, N; YANG, Y; SAIT, S. N et al.Journal of medical genetics. 2005, Vol 42, Num 8, pp 648-655, issn 0022-2593, 8 p.Article

Silencing of cdknic (p57^KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeDIAZ-MEYER, N; DAY, C. D; HIGGINS, M. J et al.Journal of medical genetics. 2003, Vol 40, Num 11, pp 797-801, issn 0022-2593, 5 p.Article