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The Beckwith-Wiedemann syndrome phenotype and the risk of cancer.
Schneid H, Vazquez MP, Vacher C, Gourmelen M, Cabrol S, Le Bouc Y. Schneid H, et al. Among authors: le bouc y. Med Pediatr Oncol. 1997 Jun;28(6):411-5. doi: 10.1002/(sici)1096-911x(199706)28:6<411::aid-mpo3>3.0.co;2-j. Med Pediatr Oncol. 1997. PMID: 9143384
[Wiedemann-Beckwith syndrome: apropos of 20 cases].
Vacher C, Vazquez MP, Le Bouc Y, Schneid H. Vacher C, et al. Among authors: le bouc y. Rev Stomatol Chir Maxillofac. 1994;95(2):192-3. Rev Stomatol Chir Maxillofac. 1994. PMID: 8036428 French. No abstract available.
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
Azzi S, Rossignol S, Steunou V, Sas T, Thibaud N, Danton F, Le Jule M, Heinrichs C, Cabrol S, Gicquel C, Le Bouc Y, Netchine I. Azzi S, et al. Among authors: le bouc y, le jule m. Hum Mol Genet. 2009 Dec 15;18(24):4724-33. doi: 10.1093/hmg/ddp435. Epub 2009 Sep 14. Hum Mol Genet. 2009. PMID: 19755383
Molecular diagnosis of Turner's syndrome.
Gicquel C, Cabrol S, Schneid H, Girard F, Le Bouc Y. Gicquel C, et al. Among authors: le bouc y. J Med Genet. 1992 Aug;29(8):547-51. doi: 10.1136/jmg.29.8.547. J Med Genet. 1992. PMID: 1355559 Free PMC article.
219 results